HistCite - index: Fragile X (expanded)

Mon Apr 4 11:08:43 2005

Papers with one of the following phrases in the title:
fragile x or FMRP or trinucleotitde expansion or nucleotide expansion or cgg

Nodes: 2647, Authors: 5321, Journals: 428, Outer References: 16458, Words: 3536
Collection span: 1967 - 2005
View: Overview. Sorted by LCS.
Page 5: 1 2 3 4 5 6 7 8 9

# LCR NCR Nodes / Date / Journal / Authors LCS GCS
1201 3 26 1278 1994 NUCLEIC ACIDS RESEARCH 22(9):1735-1740
HAN J; HSU CC; ZHU Z; LONGSHORE JW; FINLEY WH
OVER-REPRESENTATION OF THE DISEASE-ASSOCIATED (CAG) AND (CGG) REPEATS IN THE HUMAN GENOME
2 25
1202 0 0 1292 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):153-153
BLACK SH; LEVINSON G; HARTON GL; PALMER FT; SISSON ME; et al.
PREIMPLANTATION GENETIC TESTING (PGT) FOR FRAGILE-X (FRAX)
2 3
1203 11 13 1325 1995 AMERICAN JOURNAL OF MEDICAL GENETICS 55(3):384-386
PRIOR TW; PAPP AC; SNYDER PJ; SEDRA MS; GUIDA M; et al.
GERMLINE MOSAICISM AT THE FRAGILE-X LOCUS
2 7
1204 2 5 1326 1995 AMERICAN JOURNAL OF MEDICAL GENETICS 57(3):508-509
LAXOVA R
FRAGILE-X SCREENING - WHAT IS THE REAL ISSUE
2 3
1205 18 19 1331 1995 AMERICAN JOURNAL OF MEDICAL GENETICS 60(4):302-306
MUELLER OT; HARTSFIELD JK; AMAR MJA; GALLARDO LA; KOUSSEFF BG
FRAGILE-X SYNDROME - DISCORDANT LEVELS OF CGG REPEAT MOSAICISM IN 2 BROTHERS
2 5
1206 27 43 1336 1995 ARCHIVES OF DISEASE IN CHILDHOOD 72(1):3-5
TURK J
FRAGILE-X SYNDROME
2 4
1207 11 19 1339 1995 ARCHIVES OF MEDICAL RESEARCH 26:S77-S83
DiazGallardo MY; BarrosNunez P; Diaz CA; Hernandez A; GomezEspinel I; et al.
Molecular characterization of the fragile-X syndrome in the Mexican population
2 4
1208 40 112 1342 1995 BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE 1271(2-3):293-303
FLANNERY AV; HIRST MC; KNIGHT SJL; RITCHIE RJ; DAVIES KE
THE FRAGILE-X SYNDROME
2 5
1209 0 1 1353 1995 BRITISH MEDICAL JOURNAL 310(6973):148-148
CRAFT N
STUDY SUPPORTS SCREENING FOR THE FRAGILE-X-SYNDROME
2 3
1210 45 78 1355 1995 CLINICS IN LABORATORY MEDICINE 15(4):859-&
Brown WT
Perspectives and molecular diagnosis of the fragile X syndrome
2 2
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
1211 32 75 1359 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):187-198
Abrams MT; Reiss AL
Quantitative brain imaging studies of fragile X syndrome
2 3
1212 3 16 1361 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):218-222
Musumeci SA; Ferri R; Elia M; DalGracco S; Scuderi C; et al.
Sleep neurophysiology in fragile X patients
2 3
1213 5 9 1380 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):408-410
HowardPeebles PN; Maddalena A; Black SH; Levinson G; Bick DP; et al.
Fragile X screening in pediatric and obstetrical patients
2 2
1214 1 4 1391 1995 GENETIC COUNSELING 6(4):293-296
FRYNS JP
SCREENING FOR THE FRAGILE-X SYNDROME - THE NECESSITY OF INTERNATIONAL GUIDELINES FOR MOLECULAR-GENETICS PREDICTIVE TESTING IN GENERAL
2 3
1215 17 33 1393 1995 HUMAN GENETICS 96(3):323-329
DREESEN JCFM; GERAEDTS JPM; DUMOULIN JCM; EVERS JLH; PIETERS MHEC
RS46(DXS548) GENOTYPING OF REPRODUCTIVE CELLS - APPROACHING PREIMPLANTATION TESTING OF THE FRAGILE-X SYNDROME
2 7
1216 2 14 1409 1995 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 39:326-330
SIMON EW; RAPPAPORT DA; PAPKA M; WOODRUFFPAK DS
FRAGILE-X AND DOWNS-SYNDROME - ARE THERE SYNDROME-SPECIFIC COGNITIVE PROFILES AT LOW IQ LEVELS
2 4
1217 0 0 1411 1995 JOURNAL OF MEDICAL GENETICS 32(2):144-145
MORTON JE; RINDL PM; BULLOCK S; BUNDEY S; WEBB T
FRAGILE-X SYNDROME IS LESS COMMON THAN PREVIOUSLY ESTIMATED
2 2
1218 8 12 1418 1995 JOURNAL OF MEDICAL GENETICS 32(11):907-908
PINTADO E; DEDIEGO Y; HMADCHA A; CARRASCO M; SIERRA J; et al.
INSTABILITY OF THE CGG REPEAT AT THE FRAXA LOCUS AND VARIABLE PHENOTYPIC-EXPRESSION IN A LARGE FRAGILE-X PEDIGREE
2 9
1219 23 35 1436 1995 PRENATAL DIAGNOSIS 15(9):801-807
CASTELLVIBEL S; MILA M; SOLER A; CARRIO A; SANCHEZ A; et al.
PRENATAL-DIAGNOSIS OF FRAGILE-X SYNDROME - (CGG)(N) EXPANSION AND METHYLATION OF CHORIONIC VILLUS SAMPLES
2 6
1220 15 34 1448 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):1-14
Tranebjaerg L; Lubs HA; Borghgraef M; Brown WT; Fisch G; et al.
Seventh International Workshop on the Fragile X and X-linked Mental Retardation
2 4
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
1221 4 6 1492 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):377-377
HowardPeebles PN
Successful pregnancy in a fragile X carrier by donor egg
2 3
1222 13 56 1524 1996 COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY 61:689-697
Liu Q; Siomi H; Siomi MC; Fischer U; Zhang Y; et al.
Molecular characterization of the protein products of the fragile X syndrome gene and the survival of motor neurons gene
2 10
1223 7 55 1537 1996 HUMAN GENETICS 98(2):151-157
Kramer PR; Pearson CE; Sinden RR
Stability of triplet repeats of myotonic dystrophy and fragile X loci in human mutator mismatch repair cell lines
2 27
1224 28 77 1575 1996 SCREENING 4(4):175-192
Meadows KL; Sherman SL
Fragile X syndrome: Examination of issues pertaining to population-based screening
2 2
1225 8 13 1624 1997 AMERICAN JOURNAL OF MEDICAL GENETICS 72(2):245-246
Healey SC; Duffy DL; Martin NG; Turner G
Is fragile X syndrome a risk factor for dizygotic twinning?
2 4
1226 13 51 1626 1997 AMERICAN JOURNAL OF MEDICAL GENETICS 73(4):463-469
Ritchie RJ; Chakrabarti L; Knight SJL; Harding RM; Davies KE
Population genetics of the FRAXE and FRAXF GCC repeats, and a novel CGG repeat, in Xq28
2 6
1227 27 35 1640 1997 BRAZILIAN JOURNAL OF GENETICS 20(4):731-739
Mingroni-Netto RC; Pavanello RCM; Otto PA; Vianna-Morgante AM
Experience with molecular and cytogenetic diagnosis of fragile X syndrome in Brazilian families
2 2
1228 42 64 1648 1997 CURRENT OPINION IN NEUROLOGY 10(2):142-147
Chakrabarti L; Davies KE
Fragile X syndrome
2 4
1229 11 19 1657 1997 GENETIC TESTING 1(3):151-155
Das S; Kubota T; Song M; Daniel R; Berry-Kravis EM; et al.
Methylation analysis of the fragile X syndrome by PCR
2 3
1230 10 16 1663 1997 HUMAN GENETICS 101(2):186-189
Pesso R; Barkai G; Ravia Y; Gak E; Frydman M; et al.
No founder effect detected in Jewish Ashkenazi patients with fragile-X syndrome
2 4
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
1231 5 12 1690 1997 JOURNAL OF SPECIAL EDUCATION 31(3):362-376
Powell L; Houghton S; Douglas G
Comparison of etiology-specific cognitive functioning profiles for individuals with fragile X and individuals with Down syndrome
2 4
1232 8 35 1691 1997 JOURNAL OF THEORETICAL BIOLOGY 188(1):53-67
Bat O; Kimmel M; Axelrod DE
Computer simulation of expansions of DNA triplet repeats in the fragile X syndrome and Huntington's disease
2 4
1233 4 10 1709 1997 SOUTH AFRICAN MEDICAL JOURNAL 87(4):418-420
Goldman A; Krause A; Jenkins T
Fragile X syndrome occurs in the South African black population
2 4
1234 12 28 1726 1998 CLINICAL GENETICS 53(3):179-183
Chan SY; Wong V
DNA diagnosis of FRAXA and FRAXE in Chinese children with neurodevelopmental disorders and fragile X syndrome
2 5
1235 23 30 1741 1998 EUROPEAN JOURNAL OF HUMAN GENETICS 6(5):518-522
Peixoto A; dos Santos MR; Seruca R; Amorim A; Castedo S
Analysis of FMR1 and flanking microsatellite markers in normal and fragile X chromosomes in Portugal: evidence for a "protector" haplotype
2 2
1236 0 0 1813 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A269-A269
DiMarco SP; Ceman S; Torre E; Warren ST
FMRP is a phosphoprotein and a substrate of the Fes non-receptor tryosine kinase.
2 3
1237 5 20 1822 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 82(3):206-211
McConkie-Rosell A; Spiridigliozzi GA; Rounds K; Dawson DV; Sullivan JA; et al.
Parental attitudes regarding carrier testing in children at risk for fragile X syndrome
2 7
1238 4 9 1829 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):281-285
Teisl JT; Reiss AL; Mazzocco MMM
Maximizing the sensitivity of a screening questionnaire for determining fragile X at-risk status
2 2
1239 4 28 1832 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):298-301
Kotilainen J; Pirinen S
Dental maturity is advanced in fragile X syndrome
2 2
1240 19 35 1833 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):302-307
Parvari R; Mumm S; Galil A; Manor E; Bar-David Y; et al.
Deletion of 8.5 Mb, including the FMR1 gene, in a male with the fragile X syndrome phenotype and overgrowth
2 6
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
1241 6 11 1841 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):338-341
Dobkin C; Ding XH; Li SY; Houck G; Nolin SL; et al.
Accelerated prenatal diagnosis of fragile X syndrome by polymerase chain reaction restriction fragment detection
2 3
1242 8 14 1842 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):342-346
Jenkins EC; Wen GY; Kim KS; Zhong N; Sapienza VJ; et al.
Prenatal fragile X detection using cytoplasmic and nuclear-specific monoclonal antibodies
2 2
1243 21 26 1850 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):204-207
Mingroni-Netto RC; Costa SS; Angeli CB; Vianna-Morgante AM
DXS548/FRAXAC1 haplotypes in fragile X chromosomes in the Brazilian population
2 6
1244 10 14 1851 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):214-216
Pekarik V; Blazkova M; Kozak L
Haplotype analysis of the fragile X syndrome gene FMR1 in the Czech Republic
2 5
1245 4 11 1862 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):306-308
Syrrou M; Georgiou I; Patsalis PC; Bouba I; Adonakis G; et al.
Fragile X premutations and (TA)n estrogen receptor polymorphism in women with ovarian dysfunction
2 11
1246 34 44 1879 1999 CLINICAL GENETICS 55(5):346-351
Tassone F; Longshore J; Zunich J; Steinbach P; Salat U; et al.
Tissue-specific methylation differences in a fragile X premutation carrier
2 4
1247 8 12 1880 1999 CLINICAL GENETICS 56(1):98-99
Millan JM; Martinez F; Cadroy A; Gandia J; Casquero M; et al.
Screening for FMR1 mutations among the mentally retarded: prevalence of the fragile X syndrome in Spain
2 3
1248 35 50 1882 1999 CURRENT OPINION IN PSYCHIATRY 12(5):573-578
Harris SW; Hagerman RJ
Fragile X syndrome: new developments
2 2
1249 19 34 1911 1999 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 43:314-324
York A; von Fraunhofer N; Turk J; Sedgwick P
Fragile-X syndrome, Down's syndrome and autism: awareness and knowledge amongst special educators
2 4
1250 1 1 1930 1999 NATURE GENETICS 22(2):209-209
Coffee B
Acetylated histones are associated with FMR1 in normal but not fragile X-syndrome cells (vol 22, pg 98, 1999)
2 5
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
1251 14 23 1932 1999 PRENATAL DIAGNOSIS 19(13):1223-1230
Sermon K; Seneca S; Vanderfaeillie A; Lissens W; Joris H; et al.
Preimplantation diagnosis for fragile X syndrome based on the detection of the non-expanded paternal and maternal CGG
2 26
1252 3 3 1941 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(1):256-258
Hundscheid RDL; Thomas CMG; Braat DDM; Oostra BA; Smits APT
Premature ovarian failure is associated with maternally and paternally inherited premutation in Brazilian families with fragile X - Reply
2 5
1253 8 22 1968 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 92(5):336-342
McConkie-Rosell A; Spiridigliozzi GA; Sullivan JA; Dawson DV; Lachiewicz AM
Carrier testing in fragile X syndrome: Effect on self-concept
2 4
1254 16 33 1973 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 95(2):123-129
Hjalgrim H; Hansen BF; Brondum-Nielsen K; Nolting D; Kjaer I
Aspects of skeletal development in fragile X syndrome fetuses
2 4
1255 4 9 1977 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 95(5):516-517
Limprasert P; Jaruratanasirikul S; Vasiknanonte P
Unilateral macroorchidism in fragile X syndrome
2 2
1256 33 48 1979 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 97(3):183-188
Willemsen R; Oostra BA
FMRP detection assay for the diagnosis of the fragile X syndrome
2 4
1257 14 37 1982 2000 AMERICAN JOURNAL ON MENTAL RETARDATION 105(4):286-299
Kau ASM; Reider EE; Payne L; Meyer WA; Freund L
Early behavior signs of psychiatric phenotypes in fragile X syndrome
2 4
1258 22 37 1983 2000 ANNALES DE GENETIQUE 43(1):29-34
Gonzalez-del Angel A; Vidal S; Saldana Y; del Castillo V; Alcantara MA; et al.
Molecular diagnosis of the fragile X and FRAXE syndromes in patients with mental retardation of unknown cause in Mexico
2 4
1259 9 19 1988 2000 BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 275(2):608-610
Beaulieu MA
A distinct FMRP polysomal population at an advanced stage of mammalian erythropoiesis
2 2
1260 1 6 2003 2000 CYTOGENETICS AND CELL GENETICS 89(1-2):11-13
Bardoni B; Giglio S; Schenck A; Rocchi M; Mandel JL
Assignment of NUFIP1 (Nuclear FMRP Interacting Protein 1) gene to chromosome 13q14 and assignment of a pseudogene to chromosome 6q12
2 2
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
1261 8 16 2040 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:81-85
Sabaratnam M
Pathological and neuropathological findings in two males with fragile-X syndrome
2 4
1262 22 29 2072 2000 MENTAL RETARDATION 38(3):207-215
Maes B; Fryns JP; Ghesquiere P; Borghgraef M
Phenotypic checklist to screen for fragile X syndrome in people with mental retardation
2 5
1263 6 14 2081 2000 NEUROBIOLOGY OF LEARNING AND MEMORY 74(1):80-93
Irwin SA; Swain RA; Christmon CA; Chakravarti A; Weiler IJ; et al.
Evidence for altered fragile-x mental retardation protein expression in response to behavioral stimulation (vol 73, pg 87, 2000)
2 2
1264 6 26 2111 2001 AMERICAN JOURNAL OF MEDICAL GENETICS 98(1):37-45
McConkie-Rosell A; Spiridigliozzi GA; Sullivan JA; Dawson DV; Lachiewicz AM
Longitudinal study of the carrier testing process for fragile X syndrome: Perceptions and coping
2 3
1265 27 32 2125 2001 ANNALS OF CLINICAL BIOCHEMISTRY 38:264-271
Saha S; Karmakar P; Chatterjee C; Banerjee D; Das S; et al.
Fragile X syndrome in Calcutta, India
2 4
1266 35 47 2155 2001 HUMAN GENETICS 108(6):450-458
Weinhausel A; Haas OA
Evaluation of the fragile X (FRAXA) syndrome with methylation-sensitive PCR
2 6
1267 11 91 2173 2001 JOURNAL OF LEARNING DISABILITIES 34(6):520-533
Mazzocco MMM
Math learning disability and math LD subtypes: Evidence from studies of Turner syndrome, fragile X syndrome, and neurofibromatosis type 1
2 8
1268 15 47 2179 2001 JOURNAL OF SPECIAL EDUCATION 34(4):194-202
Symons FJ; Clark RD; Roberts JP; Bailey DB
Classroom behavior of elementary school-age boys with fragile X syndrome
2 3
1269 13 30 2200 2001 REVISTA DE NEUROLOGIA 33:S24-S29
Cornish K; Munir F; Wilding J
A neuropsychological and behavioural profile of a attention deficits in fragile X syndrome
2 2
1270 0 0 2218 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):185-185
Jacquemont S; Hagerman RJ; Leehey M; Greco C; Brunberg J; et al.
Characterization of a progressive neurological condition in older adult male carriers of the fragile X premutation.
2 2
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
1271 5 9 2252 2002 BRAIN & DEVELOPMENT 24(8):766-769
Incorpora G; Sorge G; Sorge A; Pavone L
Epilepsy in fragile X syndrome
2 3
1272 7 21 2254 2002 CELLULAR & MOLECULAR BIOLOGY LETTERS 7(3):877-883
Denman RB
Methylation of the arginine-glycine-rich region in the fragile X mental retardation protein FMRP differentially affects RNA binding
2 6
1273 66 84 2260 2002 CYTOGENETIC AND GENOME RESEARCH 99(1-4):257-264
Oostra BA; Willemsen R
The X chromosome and fragile X mental retardation
2 3
1274 42 139 2262 2002 DEVELOPMENTAL PSYCHOBIOLOGY 40(3):323-338
Churchill JD; Grossman AW; Irwin SA; Galvez R; Klintsova AY; et al.
A converging-methods approach to fragile X syndrome
2 8
1275 22 46 2286 2002 GENOMICS 80(4):423-432
Peier AM; Nelson DL
Instability of a premutation-sized CGG repeat in FMR1 YAC transgenic mice
2 3
1276 17 39 2291 2002 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 32(2):107-114
Fisch GS; Simensen RJ; Schroer RJ
Longitudinal changes in cognitive and adaptive Behavior scores in children and adolescents with the fragile X mutation or autism
2 3
1277 6 29 2299 2002 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 46:328-339
Kuo AY; Reiss AL; Freund LS; Huffman LC
Family environment and cognitive abilities in girls with fragile-X syndrome
2 3
1278 15 20 2310 2002 MICROSCOPY RESEARCH AND TECHNIQUE 57(3):145-147
Feng Y
Fragile X mental retardation: Misregulation of protein synthesis in the developing brain?
2 2
1279 20 42 2313 2002 MICROSCOPY RESEARCH AND TECHNIQUE 57(3):159-167
Kates WR; Folley BS; Lanham DC; Capone GT; Kaufmann WE
Cerebral growth in fragile X syndrome: Review and comparison with Down syndrome
2 6
1280 25 35 2315 2002 MICROSCOPY RESEARCH AND TECHNIQUE 57(3):174-178
Kau ASM; Meyer WA; Kaufmann WE
Early development in males with fragile X syndrome: A review of the literature
2 3
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
1281 24 59 2326 2002 NEUROBIOLOGY OF DISEASE 11(1):221-229
Castren M; Lampinen KE; Miettinen R; Koponen E; Sipola I; et al.
BDNF regulates the expression of fragile X mental retardation protein mRNA in the hippocampus
2 4
1282 8 58 2335 2002 NUCLEIC ACIDS RESEARCH 30(17):3672-3681
Weisman-Shomer P; Cohen E; Fry M
Distinct domains in the CArG-box binding factor A destabilize tetraplex forms of the fragile X expanded sequence d(CGG)(n)
2 3
1283 15 39 2385 2003 AMERICAN JOURNAL ON MENTAL RETARDATION 108(3):149-160
Abbeduto L; Murphy MM; Cawthon SW; Richmond EK; Weissman MD; et al.
Receptive language skills of adolescents and young adults with Down or fragile X syndrome
2 5
1284 14 43 2398 2003 BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 310(1):1-7
Denman RB
Deja vu all over again: FMRP binds U-rich target mRNAs
2 4
1285 20 38 2407 2003 BRAIN TOPOGRAPHY 15(3):165-171
Castren M; Paakkonen A; Tarkka IM; Ryynanen M; Partanen J
Augmentation of auditory N1 in children with fragile X syndrome
2 2
1286 69 87 2411 2003 CURRENT OPINION IN PEDIATRICS 15(6):559-566
Chiurazzi P; Neri G; Oostra BA
Understanding the biological underpinnings of fragile X syndrome
2 5
1287 28 62 2501 2004 BRAIN 127:591-601
Kogan CS; Boutet I; Cornish K; Zangenehpour S; Mullen KT; et al.
Differential impact of the FMR1 gene on visual processing in fragile X syndrome
2 2
1288 16 47 2509 2004 CURRENT BIOLOGY 14(12):1025-1034
Xu KY; Bogert BA; Li WJ; Su K; Lee A; et al.
The fragile X-related gene affects the crawling behavior of Drosophila larvae by regulating the mRNA level of the DEG/ENaC protein pickpocket1
2 3
1289 20 37 2510 2004 CURRENT BIOLOGY 14(20):1863-1870
Pan LY; Zhang YQ; Woodruff E; Broadie K
The Drosophila fragile X gene negatively regulates neuronal elaboration and synaptic differentiation
2 2
1290 23 34 2561 2004 JOURNAL OF NEUROSCIENCE 24(33):7272-7276
Stefani G; Fraser CE; Darnell JC; Darnell RB
Fragile X mental retardation protein is associated with translating polyribosomes in neuronal cells
2 3
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
1291 42 102 2575 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):60-67
Willemsen R; Oostra BA; Bassell GJ; Dictenberg J
The fragile X syndrome: From molecular genetics to neurobiology
2 5
1292 47 73 2590 2004 NATURE CELL BIOLOGY 6(11):1048-1053
Jin P; Alisch RS; Warren ST
RNA and microRNAs in fragile X mental retardation
2 3
1293 24 40 2603 2004 NUCLEIC ACIDS RESEARCH 32(7):2129-2137
Gabus C; Mazroui R; Tremblay S; Khandjian EW; Darlix JL
The fragile X mental retardation protein has nucleic acid chaperone properties
2 5
1294 0 0 10 1981 AMERICAN JOURNAL OF HUMAN GENETICS 33(6):A100-A100
CARPENTER NJ; LEICHTMAN LG; LOGAN A; SAY B
FRAGILE X-LINKED MENTAL-RETARDATION
1 1
1295 0 0 11 1981 AMERICAN JOURNAL OF HUMAN GENETICS 33(6):A107-A107
HOWARDPEEBLES PN; FINLEY WH
TESTICULAR AND CYTOGENETIC SCREENING OF RETARDED MALES FROM THE SOUTH FOR THE FRAGILE X-LINKED MENTAL-RETARDATION SYNDROME
1 1
1296 0 0 12 1981 AMERICAN JOURNAL OF HUMAN GENETICS 33(6):A122-A122
SHAPIRO LR; KUHR MD; WILMOT PL; LILIENTHAL ER; HIGGS LC
MULTIPLE SIBLING MENTAL-RETARDATION AND THE IMPACT OF THE FRAGILE X-CHROMOSOME
1 1
1297 0 0 15 1981 CANADIAN JOURNAL OF NEUROLOGICAL SCIENCES 8(2):191-191
SERGOVICH F; POZSONYI J; HINTON G
RECENT ADVANCES IN MENTAL-RETARDATION THE FRAGILE X-CHROMOSOME
1 0
1298 0 2 17 1981 CLINICAL GENETICS 19(2):140-141
SOUDEK D; GORZNY N
NO FRAGILE X-CHROMOSOME IN NORMAL MEN
1 3
1299 0 0 18 1981 CLINICAL GENETICS 19(6):493-493
NIELSEN KB; TOMMERUP N; POULSEN H; MIKKELSEN M
DANISH FAMILIES WITH X-LINKED MENTAL-RETARDATION AND FRAGILE X-CHROMOSOME
1 1
1300 0 0 35 1981 PEDIATRIC RESEARCH 15(4):569-569
SHAPIRO LR; KUHR MD; WILMOT PL
MULTIPLE SIBLING MENTAL-RETARDATION AND THE IMPACT OF THE FRAGILE X-CHROMOSOME
1 1
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
1301 0 0 36 1981 PEDIATRIC RESEARCH 15(4):645-645
PUESCHEL SM; HAYS R; MENDOZA T
A FAMILIAL X-LINKED MENTAL-RETARDATION SYNDROME ASSOCIATED WITH MULTIPLE CONGENITAL-ANOMALIES, MEGALOGENITALIA AND A FRAGILE X-CHROMOSOME
1 1
1302 0 0 42 1982 AMERICAN JOURNAL OF HUMAN GENETICS 34(6):A93-A93
HAVKIN S; CHAKI R; GOLDMAN B
FRAGILE X-CHROMOSOME IN 2 FAMILIES WITH X-LINKED MENTAL-RETARDATION
1 1
1303 0 0 43 1982 AMERICAN JOURNAL OF HUMAN GENETICS 34(6):A103-A103
NOLIN S; BROWN T; JENKINS E
FRAGILE-X SYNDROME - DILEMMAS FOR GENETIC-COUNSELING
1 1
1304 0 0 45 1982 AMERICAN JOURNAL OF HUMAN GENETICS 34(6):A121-A121
CHUDLEY AE; KNOLL J; GERRARD JW; SHEPEL L; MCGAHEY E; et al.
FRAGILE X-LINKED MENTAL-RETARDATION - EFFECT OF AGE AND INTELLIGENCE ON EXPRESSION OF FRAGILE-X
1 1
1305 0 0 48 1982 AMERICAN JOURNAL OF HUMAN GENETICS 34(6):A131-A131
KNOLL J; CHUDLEY AE; GERRARD JW
EFFICACY OF FUDR IN ENHANCING EXPRESSION OF FRA(X) IN AFFECTED MALES AND CARRIER FEMALES WITH FRAGILE X-LINKED MENTAL-RETARDATION
1 1
1306 0 0 57 1982 CLINICAL RESEARCH 30(2):A292-A292
JENKINS EC; BROWN WT; DUNCAN CJ; BROOKS J
DEMONSTRATION OF THE FRAGILE X-CHROMOSOME IN AMNIOTIC-FLUID CELLS
1 2
1307 0 0 59 1982 CLINICAL RESEARCH 30(5):A891-A891
MIXON C; DEV V
EFFECT OF FUDR AND METHIONINE ON THE EXPRESSION OF FRAGILE X IN A LYMPHOBLASTOID CELL-LINE
1 1
1308 0 0 60 1982 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 24(2):252-253
SERGOVICH F; POZSONYI J; HINTON GG
RECENT ADVANCES IN MENTAL-RETARDATION - THE FRAGILE X-CHROMOSOME
1 1
1309 1 5 61 1982 HOSPITAL PRACTICE 17(7):17-&
BROWN WT; JENKINS EC
FRAGILE X - ITS DETECTABILITY
1 1
1310 0 0 85 1982 PEDIATRICS 69(5):669-669
GERALD PS
X-LINKED MENTAL-RETARDATION AND FRAGILE-X OR MARKER-X SYNDROME - REPLY
1 1
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
1311 5 37 87 1982 WESTERN JOURNAL OF MEDICINE 137(4):278-281
MOORE BC; GLOVER TW; KAISERMCCAW B; HECHT F
FRAGILE X-LINKED MENTAL-RETARDATION AND MACRO-ORCHIDISM
1 3
1312 0 21 88 1982 WIENER KLINISCHE WOCHENSCHRIFT 94(8):217-219
FONATSCH C; FLATZ SD
FRAGILE X-CHROMOSOME AND X-LINKED MENTAL-RETARDATION
1 1
1313 0 0 102 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A146-A146
OBRIEN MM; PADREMENDOZA T; PUESCHEL SM
MATERNAL NONDISJUNCTION OF FRAGILE X-CHROMOSOME RESULTING IN KLINEFELTER SYNDROME
1 2
1314 1 1 110 1983 AMERICAN JOURNAL OF MEDICAL GENETICS 14(4):797-797
HECHT F; JACKY PB; SUTHERLAND GR
FRAGILE X-CHROMOSOME IN NORMAL MALES - REPLY
1 2
1315 2 15 115 1983 ANNALES DE GENETIQUE 26(3):171-173
JACKY PB; DILL FJ
FRAGILE-X CHROMOSOME AND CHROMOSOME CONDENSATION
1 4
1316 0 0 123 1983 CLINICAL GENETICS 23(3):236-236
PAJARES IL; DELICADO A; GALLEGO A; CASTROVIEJO IP
FAMILIAL X-LINKED MENTAL-RETARDATION AND FRAGILE X-CHROMOSOMES IN 6 SPANISH FAMILIES
1 1
1317 0 0 124 1983 CLINICAL GENETICS 23(3):241-241
NIELSEN KB; TOMMERUP N; MIKKELSEN M
CLINICAL AND CYTOGENETIC FINDINGS IN 26 MENTALLY-RETARDED MALES WITH THE FRAGILE-X
1 1
1318 0 0 125 1983 CLINICAL GENETICS 23(3):250-251
TEJADA I; NICOLAS H; CHERUY C; BOUE J
STUDY OF A LARGE SIBSHIP WITH MENTALLY-RETARDED MALES AND FEMALES CARRYING FRAGILE-X
1 1
1319 8 28 142 1983 IRISH JOURNAL OF MEDICAL SCIENCE 152(12):440-445
DEARCE MA; LAW E; MASTERSON JG
NON-SPECIFIC X-LINKED MENTAL-RETARDATION WITH FRAGILE-X CHROMOSOME - SOMATIC FEATURES, CYTOGENETIC DIAGNOSIS AND ELEMENTS FOR GENETIC-COUNSELING
1 3
1320 0 0 160 1983 PEDIATRIE 38(3):191-198
JALBERT P
FRAGILE X-LINKED MENTAL-RETARDATION - MORE QUESTIONS
1 3
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
1321 1 2 184 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):275-276
HOWARDPEEBLES PN; CARROLL AJ
RECOMBINATION BETWEEN THE FRAGILE-X AND G6PD
1 3
1322 0 0 203 1984 EUROPEAN JOURNAL OF PEDIATRICS 141(4):265-265
LARGO RH; SCHINZEL A
DEVELOPMENTAL AND BEHAVIORAL DISTURBANCES IN BOYS WITH THE FRAGILE-X SYNDROME
1 4
1323 0 1 205 1984 HUMAN GENETICS 66(1):100-100
GARDNER RJM
FRAGILE-X HOMOZYGOSITY DUE TO SOMATIC CROSSING-OVER
1 2
1324 2 10 207 1984 HUMAN GENETICS 68(2):189-190
REIDY JA; CHEN ATL
FOLIC-ACID AND CHROMOSOME BREAKAGE .2. A METHIONINE EFFECT SIMILAR TO THAT IN FRAGILE-X EXPRESSION
1 9
1325 2 6 214 1984 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 14(4):451-452
JACKSON A; HOGERMAN R; LEVITAS A
SEROTONIN LEVELS IN FRAGILE-X AUTISTIC PATIENTS
1 3
1326 1 3 217 1984 JOURNAL OF MEDICAL GENETICS 21(1):74-75
SUTHERLAND GR
ROUTINE DIAGNOSTIC-DETECTION OF THE FRAGILE X
1 4
1327 2 4 225 1984 LANCET 1(8370):220-220
JANCAR J
PREVALENCE OF FRAGILE X-CHROMOSOME
1 3
1328 3 6 235 1984 PRENATAL DIAGNOSIS 4(6):473-474
VENTER PA; COETZEE DJ; BADENHORST A; MARX MP; HOF JO; et al.
A CONFIRMED PRENATAL-DIAGNOSIS OF A FEMALE FETUS WITH THE FRAGILE X-CHROMOSOME
1 4
1329 4 12 250 1985 AMERICAN JOURNAL OF MEDICAL GENETICS 21(4):771-775
SHIMANUKI K; LIN MS; WILSON MG
REDUCTION OF FRAGILE X-EXPRESSION IN BLOOD AFTER CRYOPRESERVATION
1 3
1330 7 13 251 1985 AMERICAN JOURNAL OF MEDICAL GENETICS 22(2):415-416
BARBI G; STEINBACH P
FRAGILE-X AND MARTIN-BELL SYNDROME - NEW SOURCE OF INFORMATION
1 3
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
1331 5 14 268 1985 CLINICAL GENETICS 27(6):529-534
WEBB TP
CO-CULTIVATION STUDIES IN THE EXPRESSION OF FRAGILE(X) (Q27) IN LYMPHOCYTES
1 2
1332 3 6 270 1985 CLINICAL GENETICS 28(5):399-400
SOUDEK D
DECREASE OF FRAGILE X-FREQUENCY IN STORED-BLOOD SAMPLES - INDIVIDUAL VARIABILITY
1 1
1333 0 4 278 1985 CYTOGENETICS AND CELL GENETICS 40(1-4):726-726
PURRELLO M; ALHADEFF B; ROCCHI M; ARCHIDIACONO N; DRAYNA D; et al.
RELATIVE POSITIVE OF POLYMORPHIC DNA LOCI OF THE HUMAN X-CHROMOSOME LONG ARM SUBTELOMERIC REGION WITH RESPECT TO THE FRAGILE X SITE (FRAXQ27)
1 4
1334 3 5 291 1985 HUMAN GENETICS 71(2):182-182
PEMBREY ME; WINTER RM
FURTHER SEGREGATION ANALYSIS OF THE FRAGILE X-SYNDROME WITH SPECIAL REFERENCE TO TRANSMITTING MALES
1 1
1335 2 3 292 1985 HUMAN GENETICS 71(2):183-183
SHERMAN SL; JACOBS PA; MORTON NE
FURTHER SEGREGATION ANALYSIS OF THE FRAGILE X-SYNDROME WITH SPECIAL REFERENCE TO TRANSMITTING MALES - REPLY
1 1
1336 2 2 297 1985 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 6(5):322-322
KERBESHIAN J; BURD L; MARTSOLF JT
THE MULTIPOTENTIAL OUTCOME OF FRAGILE X-SYNDROME
1 1
1337 1 4 316 1986 AMERICAN JOURNAL OF DISEASES OF CHILDREN 140(4):327-327
BOWERS EJ
FRAGILE-X SYNDROME AND LEARNING-DISABILITIES
1 2
1338 1 7 317 1986 AMERICAN JOURNAL OF DISEASES OF CHILDREN 140(4):327-328
HAGERMAN RJ
FRAGILE-X SYNDROME AND LEARNING-DISABILITIES - REPLY
1 1
1339 4 4 346 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):527-530
TOMMERUP N; HOLMGREN G; STEINBACH P
FRAGILE-X - CARRIER DETECTION IN PREGNANCY
1 4
1340 4 18 348 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):537-544
NIELSEN KB
SEX-CHROMOSOME ANEUPLOIDY IN FRAGILE-X CARRIERS
1 6
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
1341 0 0 379 1986 CLINICAL GENETICS 29(5):462-462
GOONEWARDENA P; GUSTAVSON KH; HOLMGREN G; TOLUN A; CHOTAI J; et al.
STUDIES ON FRAGILE X-MENTAL RETARDATION BY THE USE OF DNA PROBES
1 1
1342 2 4 380 1986 CLINICAL GENETICS 29(5):475-475
TOMMERUP N
THE FRAGILE X-CHROMOSOME - PRENATAL-DIAGNOSIS
1 3
1343 0 0 409 1986 PEDIATRIC RESEARCH 20(4):A269-A269
MURPHY PD; WATSON MS; KIDD KK; BREG WR
MOLECULAR APPROACHES TO CARRIER DETECTION AND PRENATAL-DIAGNOSIS OF THE FRAGILE-X SYNDROME (MCKUSICK NUMBER 30920)
1 2
1344 1 4 416 1987 AMERICAN JOURNAL OF DISEASES OF CHILDREN 141(6):601-601
BARTOLUCCI G; SZATMARI P
POSSIBLE SIMILARITIES BETWEEN THE FRAGILE-X AND ASPERGERS SYNDROMES
1 2
1345 1 1 417 1987 AMERICAN JOURNAL OF DISEASES OF CHILDREN 141(6):601-602
HAGERMAN RJ
POSSIBLE SIMILARITIES BETWEEN THE FRAGILE-X AND ASPERGERS SYNDROMES - REPLY
1 1
1346 1 4 436 1987 BRITISH MEDICAL JOURNAL 295(6603):922-922
MCKINLEY MJ; NICOLAIDES KH; KEARNEY LU; HERON O
FRAGILE-X SYNDROME
1 3
1347 10 29 437 1987 CLINICAL CHEMISTRY 33(10):1726-1730
THIBODEAU SN
USE OF RESTRICTION-FRAGMENT-LENGTH-POLYMORPHISM ANALYSIS FOR DETECTING CARRIERS OF FRAGILE-X SYNDROME
1 1
1348 12 23 443 1987 CYTOGENETICS AND CELL GENETICS 44(2-3):118-122
LIN MS; SHIMANUKI K; WILSON MG
EXPRESSION OF FRAGILE-X IN HUMAN-MOUSE SOMATIC-CELL HYBRIDS
1 1
1349 0 0 444 1987 CYTOGENETICS AND CELL GENETICS 46(1-4):587-587
BROWN WT; WU Y; GROSS AC; CHAN CB; DOBKIN CS; et al.
LINKAGE OF FLANKING PROBES IN 40 FRAGILE X-FAMILIES
1 7
1350 0 0 448 1987 CYTOGENETICS AND CELL GENETICS 46(1-4):688-689
SCHWARTZ C; PATTERSON M; DAVIES K; TRUNCA C; TRASK B; et al.
THE USE OF DISTAL DELETIONS OF XQ TO ORDER LOCI BETWEEN FACTOR-IX AND THE FRAGILE-X SITE (XQ27.3)
1 2
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
1351 6 9 452 1987 GENETIKA 23(3):504-509
SULEIMANOVA DG; KULESHOV NP
SPONTANEOUS AND INDUCED CHROMOSOMAL INSTABILITY IN PATIENTS WITH FRAGILE X-CHROMOSOME, SUFFERING FROM X-LINKED MENTAL-RETARDATION
1 3
1352 0 0 478 1987 JOURNAL OF MEDICAL GENETICS 24(10):640-640
SENIOR J; KILPATRICK M; WEBB T
COMPARATIVE LINKAGE STUDIES IN THE FRAGILE X-SYNDROME
1 1
1353 0 0 479 1987 JOURNAL OF MEDICAL GENETICS 24(10):641-641
HULTEN M; JOHANNISSON R
MEIOSIS IN THE FRAGILE-X MENTAL-RETARDATION SYNDROME
1 1
1354 2 4 481 1987 JOURNAL OF MENTAL DEFICIENCY RESEARCH 31:81-85
COWIE VA; SINGH KR; WHEATER R; BIRD J
THE FRAGILE-X SYNDROME IN TWIN SISTERS
1 1
1355 1 2 487 1987 LANCET 2(8554):329-329
VERLOES A; SACRE JP; GEUBELLE F
SOTOS SYNDROME AND FRAGILE-X CHROMOSOMES
1 5
1356 0 1 489 1987 NEW ENGLAND JOURNAL OF MEDICINE 316(8):483-483
TURNER G
THE FRAGILE X-CHROMOSOME - REPLY
1 1
1357 0 0 490 1987 NEW ENGLAND JOURNAL OF MEDICINE 316(8):483-483
HECHT F; HECHT BK
THE FRAGILE X-CHROMOSOME
1 1
1358 4 4 491 1987 NEW ENGLAND JOURNAL OF MEDICINE 316(8):483-483
BURD L
THE FRAGILE X-CHROMOSOME
1 1
1359 0 0 494 1987 PRACTITIONER 231(1431):910-&
BUNDEY S
THE FRAGILE X-SYNDROME
1 1
1360 0 0 498 1987 TERATOLOGY 36(3):453-453
SUZUKI Y; CHYO H; MATSUI A; SHIMOMURA C; FUNAHASI M
CLINICAL-DIAGNOSIS OF FRAGILE-X SYNDROME
1 2
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
1361 0 0 505 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):20-21
KEREM B; GOITEIN R; SCHAAP T
THE DISTRIBUTION OF FRAGILE-X CHROMOSOMES IN AMNIOTIC CELLS CULTURED BY THE INSITU TECHNIQUE
1 1
1362 6 11 522 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):177-183
MILONE G; CONTI L; RIZZO R; SANFILIPPO S; SAMMITO V; et al.
A DERMATOGLYPHIC STUDY OF A GROUP OF SICILIAN CHILDREN WITH FRAGILE-X SYNDROME
1 2
1363 1 3 524 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):201-205
BROWN WT; RUDELLI RD; WISNIEWSKI HM
FRAGILE-X SYNDROME - NEUROPATHOLOGY CENTER
1 1
1364 2 8 527 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):231-236
SUTHERS GK; TURNER G; MULLEY JC
CASE-REPORT - FRAGILE-X SYNDROME AND NEPHROGENIC DIABETES-INSIPIDUS
1 2
1365 1 7 539 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):443-450
NOLIN SL; JENKINS EC; BROWN WT; DOBKIN CS
INSITU NICK TRANSLATION OF THE FRAGILE-X REGION
1 2
1366 17 31 576 1988 CLINICAL GENETICS 33(6):410-417
VEENEMA H; BEVERSTOCK GC; DEKONING T; PEARSON PL; VANDEKAMP JJP
THE FRAGILE X-CHROMOSOME - AN EVALUATION OF THE RESULTS IN A ROUTINE CYTOGENETIC LABORATORY IN THE PERIOD 1981-1986
1 3
1367 7 32 580 1988 CYTOGENETICS AND CELL GENETICS 47(4):177-180
HORI T; TAKAHASHI E; TSUJI H; TSUJI S; MURATA M
FRAGILE-X EXPRESSION IN THYMIDINE-PROTOTROPHIC AND AUXOTROPHIC HUMAN-MOUSE SOMATIC-CELL HYBRIDS UNDER LOW AND HIGH THYMIDYLATE STRESS CONDITIONS
1 3
1368 2 17 590 1988 HUMAN GENETICS 79(3):231-234
JOHANNISSON R; FROSTERISKENIUS U; SAADALLAH N; HULTEN MA
SPERMATOGENESIS IN 2 PATIENTS WITH THE FRAGILE-X SYNDROME .2. 1ST MEIOSIS - LIGHT AND ELECTRON-MICROSCOPY
1 3
1369 10 48 592 1988 HUMAN GENETICS 79(4):341-346
VANDAMME B; LIEBAERS I; HENS L; BERNHEIM JL; ROOBOL C
THE ROLE OF FLUORINATED PYRIMIDINE ANALOGS IN THE INDUCTION OF THE INVITRO EXPRESSION OF THE FRAGILE X-CHROMOSOME
1 1
1370 27 63 612 1988 QUARTERLY JOURNAL OF MEDICINE 69(258):755-763
FROSTERISKENIUS U; PATTERSON MN; BELL MV; BLOOMFIELD J; DAVIES KE
MOLECULAR ANALYSIS OF THE FRAGILE-X SYNDROME
1 1
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
1371 3 31 613 1988 SCHIZOPHRENIA RESEARCH 1(4):277-281
DELISI LE; REISS AL; WHITE BJ; GERSHON ES
CYTOGENETIC STUDIES OF MALES WITH SCHIZOPHRENIA - SCREENING FOR THE FRAGILE X-CHROMOSOME AND OTHER CHROMOSOMAL-ABNORMALITIES
1 36
1372 0 0 615 1989 AMERICAN FAMILY PHYSICIAN 39(5):185-193
SIMENSEN RJ; ROGERS RC
FRAGILE-X SYNDROME
1 1
1373 4 53 628 1989 AMERICAN ZOOLOGIST 29(2):569-591
LAIRD CD
FROM POLYTENE CHROMOSOMES TO HUMAN EMBRYOLOGY - CONNECTIONS VIA THE HUMAN FRAGILE-X SYNDROME
1 3
1374 6 8 630 1989 ARCHIVES OF DISEASE IN CHILDHOOD 64(9):1223-1224
WINTER RM
FRAGILE-X MENTAL-RETARDATION
1 3
1375 2 10 637 1989 CYTOGENETICS AND CELL GENETICS 50(2-3):172-173
SAUER SM; PHELAN MC; RICHER CL; SCHWARTZ CE
PHYSICAL MAPPING OF PROBES PROXIMAL TO THE FRAGILE-X LOCUS (FRAX) CONFIRMS THE ORDER F9-DXS105 (CX55.7)-DXS98 (4D8)-FRAXA
1 1
1376 0 0 662 1989 NEUROLOGIC CLINICS 7(1):107-121
BROWN WT
THE FRAGILE-X SYNDROME
1 1
1377 21 41 667 1989 PSYCHOLOGY IN THE SCHOOLS 26(4):380-389
SIMENSEN RJ; ROGERS RC
SCHOOL-PSYCHOLOGY AND MEDICAL DIAGNOSIS - THE FRAGILE X-SYNDROME
1 1
1378 2 3 671 1989 ZEITSCHRIFT FUR KINDER-UND JUGENDPSYCHIATRIE UND PSYCHOTHERAPIE 17(2):85-90
BLANK R
MAIN SYMPTOMS - DELAYED LANGUAGE-DEVELOPMENT AND BEHAVIOR PROBLEMS - 2 CASE-REPORTS ON THE FRAGILE-X SYNDROME
1 1
1379 30 39 672 1989 ZEITSCHRIFT FUR KINDER-UND JUGENDPSYCHIATRIE UND PSYCHOTHERAPIE 17(2):91-97
VONGONTARD A
PSYCHOPATHOLOGY ASSOCIATED WITH THE FRAGILE-X SYNDROME
1 2
1380 0 0 673 1989 ZHURNAL NEVROPATOLOGII I PSIKHIATRII IMENI S S KORSAKOVA 89(8):101-105
BLYUMINA MG
CLINICAL SIGNS OF OLIGOPHRENIA WITH FRAGILE X-CHROMOSOME IN PREPUBERTY AND POSTPUBERTY MALES
1 2
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
1381 12 20 682 1990 AMERICAN JOURNAL OF HUMAN GENETICS 47(6):988-993
OHASHI H; KUWANO A; TSUKAHARA M; ARINAMI T; KAJII T
REPLICATION PATTERNS OF THE FRAGILE-X IN HETEROZYGOUS CARRIERS - ANALYSIS BY A BRDURD ANTIBODY METHOD
1 2
1382 6 13 699 1990 BRITISH JOURNAL OF HOSPITAL MEDICINE 43(1):17-17
BUNDEY S
FRAGILE-X SYNDROME
1 1
1383 6 12 706 1990 HUMAN GENETICS 84(2):216-217
BUTLER MG
NO SIGNIFICANT RELATIONSHIP BETWEEN AGE AND FREQUENCY OF CHROMOSOME LESIONS IN MENTALLY-RETARDED INDIVIDUALS WITH OR WITHOUT THE FRAGILE X-SYNDROME
1 4
1384 1 4 720 1990 JOURNAL OF NEUROLOGY 237(1):65-66
MUSUMECI SA; FERRI R; BERGONZI P
THE SPECIFICITY OF THE CHARACTERISTIC SLEEP EEG PATTERN IN THE FRAGILE-X SYNDROME
1 1
1385 0 2 730 1990 NUCLEIC ACIDS RESEARCH 18(3):692-692
HUPKES PE; VANBENNEKOM CA; VANOOST BA; OOSTRA BA
RN1, A NEW POLYMORPHIC MARKER NEAR THE FRAGILE-X LOCUS - (HGM10 ASSIGNMENT DXS-369)
1 2
1386 2 3 736 1990 PRENATAL DIAGNOSIS 10(8):545-546
OOSTRA BA; SANDKUYL LA; HALLEY DJJ
RISK CALCULATION OF MISSED PRENATAL-DIAGNOSIS OF FRAGILE-X SYNDROME
1 1
1387 0 0 761 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):231-231
SHAPIRO LR; WILMOT PL
PRENATAL CYTOGENETIC DIAGNOSIS OF THE FRAGILE X-SYNDROME - DETERMINATION OF ACCURACY
1 1
1388 12 39 787 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):158-172
BROWN WT; JENKINS E; NERI G; LUBS H; SHAPIRO LR; et al.
4TH INTERNATIONAL WORKSHOP ON THE FRAGILE-X AND X-LINKED MENTAL-RETARDATION
1 7
1389 1 8 794 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):288-289
ZHAO Y; SHEN Y; LIU Y; ZHANG JC; YE LZ; et al.
FRAGILE-X SYNDROME (MARTIN-BELL SYNDROME) IN CHINA
1 1
1390 7 20 798 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):311-318
CARPENTER NJ
DNA LINKAGE ANALYSIS OF 26 FAMILIES WITH FRAGILE-X SYNDROME
1 1
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
1391 14 31 800 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):322-327
GOONEWARDENA P; BROWN WT; GROSS AC; FERRANDO C; DOBKIN C; et al.
LINKAGE ANALYSIS OF THE FRAGILE-X SYNDROME USING A NEW DNA MARKER U6.2 DEFINING LOCUS DXS304
1 1
1392 3 20 802 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):343-346
BROWN WT; GROSS AC; GOONEWARDENA P; FERRANDO C; DOBKIN C; et al.
LINKAGE IN FRAGILE-X FAMILIES OF 3 DISTAL FLANKING MARKERS - ST14, DX13, AND F8
1 2
1393 1 7 816 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):416-417
JENKINS LS; GRUENERT DC; JENKINS EC; SCHONBERG SA
TRANSFORMATION AND ESTABLISHMENT OF FRAGILE-X CELL-LINES FROM AMNIOCYTES
1 1
1394 6 20 819 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):429-433
KIMCHISARFATY C; GOITEIN R; KEREM B; WERNER M; MEIDAN B; et al.
ENDOREDUPLICATION AND POLYPLOIDY IN FRAGILE-X CELLS INDUCED BY METHOTREXATE AND FLUORODEOXYURIDINE - IMPLICATIONS FOR DIAGNOSIS
1 3
1395 2 33 823 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):456-463
KRAWCZUN MS; JENKINS EC; DUNCAN CJ; STARKHOUCK SL; KUNAPORN S; et al.
DISTRIBUTION OF AUTOSOMAL FRAGILE SITES IN SPECIMENS CULTURED FOR PRENATAL FRAGILE-X DIAGNOSIS
1 1
1396 1 8 824 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):464-466
JENKINS EC; BROOKS SE; STARKHOUCK SL; DUNCAN CJ; BROOKS SLS; et al.
SV40-TRANSFORMED FRAGILE(X) AMNIOCYTES
1 1
1397 16 38 842 1991 BIOESSAYS 13(5):243-251
JORDAN BR
FRAGILE X-LINKED MENTAL-RETARDATION AND THE DIFFICULTIES OF REVERSE GENETICS
1 1
1398 0 0 855 1991 CYTOGENETICS AND CELL GENETICS 56(3-4):221-221
SHAPIRO LR; EALLONARDO SJ; WILMOT PL
INTERNAL CONTROL FOR SUCCESSFUL INDUCTION OF THE FRAGILE X-CHROMOSOME - OTHER FOLATE SENSITIVE FRAGILE SITE EXPRESSION ELIMINATED
1 1
1399 2 9 856 1991 CYTOGENETICS AND CELL GENETICS 58(3-4):2054-2055
BOUVET A; BASRUR PK
A MARKER FRAGILE X-CHROMOSOME ASSOCIATED WITH BALDY CALF SYNDROME
1 1
1400 1 3 863 1991 CYTOGENETICS AND CELL GENETICS 58(3-4):2085-2085
RIGGINS GJ; SHERMAN SL; OOSTRA BA; FEITELL D; SUTCLIFFE JS; et al.
A HIGHLY POLYMORPHIC DINUCLEOTIDE REPEAT, DXS 548, IS TIGHTLY LINKED TO THE FRAGILE-X SITE
1 2
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
1401 9 23 866 1991 GENOMICS 10(4):1053-1060
DJABALI M; NGUYEN C; BIUNNO I; OOSTRA BA; MATTEI MG; et al.
LASER MICRODISSECTION OF THE FRAGILE X REGION - IDENTIFICATION OF COSMID CLONES AND OF CONSERVED SEQUENCES IN THIS REGION
1 25
1402 6 9 876 1991 JOURNAL OF MEDICAL GENETICS 28(12):811-813
CONNOR JM
CLONING OF THE GENE FOR THE FRAGILE-X SYNDROME - IMPLICATIONS FOR THE CLINICAL GENETICIST
1 1
1403 3 12 890 1991 NATURE 349(6312):742-743
CRAIG I
HUMAN-GENETICS - METHYLATION AND THE FRAGILE-X
1 5
1404 0 16 901 1991 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 88(3):921-925
OBA T; ANDACHI Y; MUTO A; OSAWA S
CGG - AN UNASSIGNED OR NONSENSE CODON IN MYCOPLASMA-CAPRICOLUM
1 49
1405 8 14 912 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 42(2):184-186
FINUCANE BM; JAEGER E; DUNN E; SCOTT CI
STUDY OF COLOR-VISION IN FRAGILE-X SYNDROME
1 1
1406 10 14 929 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):136-141
JENKINS EC; GENOVESE MJ; DUNCAN CJ; GU H; STARKHOUCK SL; et al.
FRA(X)(Q27.2), THE COMMON FRAGILE SITE, OBSERVED IN ONLY ONE OF 760 CASES STUDIED FOR THE FRAGILE-X SYNDROME
1 1
1407 11 21 930 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):142-148
FISCH GS; FRYNS JP
FACTORS WHICH CONTRIBUTE TO CYTOGENETIC FREQUENCY OF EXPRESSION IN FAMILIES OF FRAGILE-X FEMALES
1 1
1408 12 19 931 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):155-160
JENKINS EC; DUNCAN CJ; GU H; GENOVESE M; KRAWCZUN MS
DIALYZED FETAL BOVINE SERUM INCREASES CYTOGENETIC FRAGILE-X EXPRESSION
1 1
1409 4 6 935 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):170-173
SHAPIRO LR; WILMOT PL; FISCH GS
PRENATAL CYTOGENETIC DIAGNOSIS OF THE FRAGILE-X SYNDROME IN AMNIOTIC-FLUID - CALCULATION OF ACCURACY
1 1
1410 11 12 937 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):181-186
MURPHY PD; WILMOT PL; SHAPIRO LR
PRENATAL-DIAGNOSIS OF FRAGILE-X SYNDROME - RESULTS FROM PARALLEL MOLECULAR AND CYTOGENETIC STUDIES
1 1
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
1411 7 22 951 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):312-319
CARPENTER NJ; SWARTZBOYD J; PRICHARD JK; LAM T
LINKAGE AND RISK ASSESSMENT IN FRAGILE-X FAMILIES USING NEW DNA PROBES AT XQ27
1 1
1412 5 5 955 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):339-344
VIANNAMORGANTE AM; OTTO PA
NOTES ON THE POPULATION-GENETICS OF FRAGILE X SYNDROME
1 1
1413 12 25 963 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 44(5):676-682
STROM CM; BRUSCA RM; PIZZI WJ
DOUBLE-BLIND, PLACEBO-CONTROLLED CROSSOVER STUDY OF FOLINIC ACID (LEUCOVORIN(R)) FOR THE TREATMENT OF FRAGILE-X SYNDROME
1 3
1414 3 4 971 1992 ARCHIVES FRANCAISES DE PEDIATRIE 49(5):477-477
DROUIN V; VANNIER JP; MOIROT H; MITROFANOFF P; TRON P
WILMS-TUMOR AND FRAGILE-X SYNDROME
1 1
1415 5 11 975 1992 BRITISH MEDICAL JOURNAL 305(6847):208-208
MOORE DWY
NEW DEVELOPMENTS IN THE FRAGILE-X SYNDROME
1 1
1416 16 33 984 1992 EDUCATIONAL RESEARCH 34(3):221-228
GIBB C
THE MOST COMMON-CAUSE OF LEARNING-DIFFICULTIES - A PROFILE OF FRAGILE-X SYNDROME AND ITS IMPLICATIONS FOR EDUCATION
1 1
1417 7 8 1002 1992 JOURNAL OF MEDICAL GENETICS 29(10):726-729
TARLETON J; WONG S; HEITZ D; SCHWARTZ C
DIFFICULT DIAGNOSIS OF THE FRAGILE X-SYNDROME MADE POSSIBLE BY DIRECT DETECTION OF DNA MUTATIONS
1 1
1418 8 9 1004 1992 JOURNAL OF MEDICAL GENETICS 29(12):919-920
TARLETON J; WONG S; SCHWARTZ C
DIRECT ANALYSIS OF THE FMR-1 GENE PROVIDES AN EXPLANATION FOR AN EXCEPTIONAL CASE OF A FRAGILE-X NEGATIVE, MENTALLY-RETARDED MALE IN A FRAGILE-X FAMILY
1 2
1419 19 25 1005 1992 JOURNAL OF PEDIATRICS 121(3):385-390
POTTER NT; LOZZIO CB; ANDERSON IJ; BOWLIN ES; MATTESON KJ
USE OF A MOLECULAR GENETIC APPROACH TO DIAGNOSING THE FRAGILE-X GENOTYPE
1 1
1420 17 25 1011 1992 MEDICINA CLINICA 98(4):121-124
GINE R; ESPINAS ML; ANTICH J; CARBALLO M
MOLECULAR-GENETICS OF THE FRAGILE-X SYNDROME - MOLECULAR DIAGNOSIS BY DNA PROBES
1 1
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
1421 27 59 1025 1992 PSYCHIATRIC GENETICS 2(4):277-300
BOLTON P; PICKLES A; BUTLER L; SUMMERS D; WEBB T; et al.
FRAGILE-X IN FAMILIES MULTIPLEX FOR AUTISM AND RELATED PHENOTYPES - PREVALENCE AND CRITERIA FOR CYTOGENETIC DIAGNOSIS
1 7
1422 19 26 1028 1992 ZEITSCHRIFT FUR KINDER-UND JUGENDPSYCHIATRIE UND PSYCHOTHERAPIE 20(2):113-120
VONGONTARD A; HILLIG U; HEROLD D
CLINICAL AND CYTOGENETIC PROBLEMS IN THE DIAGNOSIS OF THE FRAGILE-X SYNDROME
1 1
1423 4 9 1029 1992 ZHURNAL NEVROPATOLOGII I PSIKHIATRII IMENI S S KORSAKOVA 92(4):28-31
LASTOCHKINA NA; KUPRIYANOVA TA; PUCHINSKAYA LM; MARINCHEVA GS; GORKOVA SA
THE CLINICOELECTROPHYSIOLOGICAL CHARACTERIZATION OF WOMEN, HETEROZYGOUS CARRIERS OF FRAGILE X-CHROMOSOME
1 1
1424 23 29 1033 1993 AMERICAN JOURNAL OF DISEASES OF CHILDREN 147(11):1231-1235
RAMOS FJ; EUNPU DL; FINUCANE B; PFENDNER EG
DIRECT DNA TESTING FOR FRAGILE-X SYNDROME
1 2
1425 0 0 1040 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):78-78
ROUSSEAU F; HEITZ D; TARLETON J; MACPHERSON J; PETTERSON U; et al.
A COLLABORATIVE MULTICENTER STUDY OF DIRECT DIAGNOSIS OF THE FRAGILE-X SYNDROME WITH PROBE STB12.3 - THE 1ST 2253 CASES
1 1
1426 0 0 1043 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):144-144
HAGERMAN R; HULL C; CARPENTER I; STALEY L; OCONNOR R; et al.
HIGH-FUNCTIONING FRAGILE X MALES
1 1
1427 0 0 1047 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):448-448
HOLDEN JJA; CHALIFOUX M; WING M; WHITE BN; GLOVER T; et al.
THE FRAGILE-X SYNDROME AND PREMATURE MENOPAUSE
1 1
1428 0 0 1050 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):678-678
EBERHART DE; WARREN ST
ABNORMAL CHROMATIN STRUCTURE ASSOCIATED WITH THE FULL FRAGILE-X MUTATION
1 2
1429 0 0 1051 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):717-717
PERGOLIZZI RG; ERSTER SH; MILLAN CA; GUZOWSKI DE; SELLATI LM
STABILITY OF THE CGG REPEAT REGION OF FMR-1
1 1
1430 0 0 1063 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):1241-1241
TORRES W; SAHOTA A; BOYADJIEV S; VANCE GH; WEAVER DD
FRAGILE-X FULL MUTATION IN 2 CLINICALLY UNAFFECTED BROTHERS
1 2
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
1431 0 0 1082 1993 ANNALES DE PEDIATRIE 40(9):565-572
BLANC DS; DANGELO J; ETANGS NLD
AUTISM AND THE FRAGILE X-SYNDROME
1 1
1432 0 0 1120 1993 IRISH MEDICAL JOURNAL 86(3):92-&
KEENAN E; KEANE V; RAMSEY L
FRAGILE-X SYNDROME - A REVIEW
1 1
1433 10 11 1132 1993 JOURNAL OF MEDICAL GENETICS 30(3):193-197
KNOBLOCH O; PELZ F; WICK U; NELSON DL; ZOLL B
DIRECT VERSUS INDIRECT MOLECULAR DIAGNOSIS OF FRAGILE-X MENTAL-RETARDATION IN 40 GERMAN FAMILIES AT RISK
1 1
1434 7 9 1137 1993 JOURNAL OF MEDICAL GENETICS 30(9):785-787
SUZUMORI K; YAMAUCHI M; SEKI N; KONDO I; HORI T
PRENATAL-DIAGNOSIS OF A HYPERMETHYLATED FULL FRAGILE-X MUTATION IN CHORIONIC VILLI OF A MALE FETUS
1 5
1435 6 7 1143 1993 LANCET 342(8878):1004-1005
YOUNG ID
DIAGNOSING FRAGILE-X SYNDROME
1 1
1436 17 34 1146 1993 MEDICAL JOURNAL OF AUSTRALIA 158(7):482-485
SUTHERLAND GR; MULLEY JC; RICHARDS RI
FRAGILE-X SYNDROME - THE MOST COMMON CAUSE OF FAMILIAL INTELLECTUAL HANDICAP
1 5
1437 3 6 1185 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):374-377
STEYAERT J; BORGHGRAEF M; FRYNS JP
APPARENTLY ENHANCED VISUAL INFORMATION-PROCESSING IN FEMALE FRAGILE-X CARRIERS - PRELIMINARY FINDINGS
1 1
1438 4 7 1190 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):403-404
SCHAAP C; FRYNS JP
SEVERE PROGRESSIVE NEUROLOGICAL DISORDER ASSOCIATED WITH HYDROCEPHALUS IN A MAN WITH FRAGILE-X-SYNDROME
1 2
1439 5 8 1193 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):436-442
JENKINS EC; MORYS I; HENDERSON J; GENOVESE M; CARTER M; et al.
FRAGILE-X INDUCTION SYSTEMS IN CVS CULTURES - EFFECT ON CYTOGENETIC, PCR, AND GENOMIC SOUTHERN BLOT DNA ANALYSES OF THE FMR-1 GENE
1 1
1440 7 8 1197 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):452-453
JENKINS EC; GENOVESE M; DUNCAN CJ; GU H; STARKHOUCK S; et al.
OCCURRENCE OF ANEUPLOIDY FOR THE X-CHROMOSOME IN OVER 1,300 UNRELATED SPECIMENS SCREENED FOR THE FRAGILE X-CHROMOSOME
1 1
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
1441 14 17 1215 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 53(4):370-373
PUISSANT H; MALINGE MC; LARGETPIET A; MARTIN D; CHAUVEAU P; et al.
MOLECULAR ANALYSIS OF 53 FRAGILE-X FAMILIES WITH THE PROBE-STB12.3
1 2
1442 9 28 1218 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 54(2):141-143
CRADDOCK N; DANIELS J; MCGUFFIN P; OWEN M
VARIATION AT THE FRAGILE X-LOCUS DOES NOT INFLUENCE SUSCEPTIBILITY TO BIPOLAR DISORDER
1 6
1443 14 28 1224 1994 BRITISH JOURNAL OF CLINICAL PRACTICE 48(1):42-44
PATEL BD
THE FRAGILE-X SYNDROME
1 1
1444 1 16 1226 1994 CANCER RESEARCH 54(19):5212-5216
LEE ST; MCGLENNEN RC; LITZ CE
CLONAL DETERMINATION BY THE FRAGILE-X (FMR1) AND PHOSPHOGLYCERATE KINASE (PGK) GENES IN HEMATOLOGICAL MALIGNANCIES
1 12
1445 0 19 1234 1994 GENES CHROMOSOMES & CANCER 9(2):141-144
RIGGINS GJ; SHERMAN SL; PHILLIPS CN; STOCK W; WESTBROOK CA; et al.
CGG-REPEAT POLYMORPHISM OF THE BCR GENE RULES OUT PREDISPOSING ALLELES LEADING TO THE PHILADELPHIA-CHROMOSOME
1 8
1446 1 1 1249 1994 JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION 271(1):28-28
BROWN WT; HOUCK GE; JEZIOROWSKA A; LEVINSON FN; DING X; et al.
RAPID FRAGILE-X CARRIER SCREENING AND PRENATAL-DIAGNOSIS USING A NONRADIOACTIVE PCR TEST (VOL 270, PG 1569, 1993)
1 1
1447 9 20 1256 1994 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 38:1-8
DEVRIES LBA; HALLEY DJJ; OOSTRA BA; NIERMEIJER MF
THE FRAGILE-X SYNDROME - A GROWING GENE CAUSING FAMILIAL INTELLECTUAL DISABILITY
1 2
1448 1 2 1263 1994 JOURNAL OF MEDICAL GENETICS 31(10):820-820
DEVRIES BBA; NIERMEIJER MF
THE PRADER-WILLI-LIKE PHENOTYPE IN FRAGILE-X PATIENTS - A DESIGNATION FACILITATING CLINICAL (AND MOLECULAR) DIFFERENTIAL-DIAGNOSIS
1 6
1449 6 12 1264 1994 JOURNAL OF MEDICAL GENETICS 31(12):950-952
CURTIS G; DENNIS N; MACPHERSON J
THE IMPACT OF GENETIC-COUNSELING ON FEMALES IN FRAGILE-X FAMILIES
1 1
1450 0 0 1279 1994 PEDIATRIC RESEARCH 35(4):A23-A23
LACHIEWICZ AM; DAWSON DV
AUTISTIC BEHAVIORS OF YOUNG GIRLS WITH FRAGILE X-SYNDROME
1 1
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
1451 10 22 1362 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):223-229
King RA; Hagerman R; Houghton M
Ocular findings in fragile X syndrome
1 1
1452 27 36 1363 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):230-241
Brun C; Obiols JE; Cheema A; OConnor R; Riddle J; et al.
Longitudinal IQ changes in fragile X females
1 1
1453 26 41 1368 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):293-301
Jenkins EC; Houck GE; Ding XH; Li SY; StarkHouck SL; et al.
An update on fragile X prenatal diagnosis: End of the cytogenetic testing era
1 1
1454 2 9 1390 1995 GENETIC COUNSELING 6(3):207-210
ALEMBIK Y; DOTT B; STOLL C
RETT-LIKE SYNDROME IN FRAGILE-X SYNDROME
1 6
1455 12 26 1392 1995 GENETIC EPIDEMIOLOGY 12(3):279-290
HUGGINS RM; LOESCH DZ
USE OF ROBUST STATISTICAL-METHODS TO DETERMINE THE EFFECT OF FRAGILE-X ON MEANS AND VARIANCE-COMPONENTS OF A QUANTITATIVE TRAIT
1 2
1456 8 11 1399 1995 ISRAEL JOURNAL OF MEDICAL SCIENCES 31(5):323-325
DAR H; SCHAAP T; BAITOR H; BOROCHOWITZ Z; GELMANKOHAN Z; et al.
ETHNIC DISTRIBUTION OF THE FRAGILE-X SYNDROME IN ISRAEL - EVIDENCE OF FOUNDER CHROMOSOMES()
1 1
1457 4 21 1456 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):27-30
Carrel L; Willard HF
An assay for X inactivation based on differential methylation at the fragile X locus, FMR1
1 32
1458 9 10 1459 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):187-190
Grasso M; Perroni L; Colella S; Piombo G; Argusti A; et al.
Prenatal diagnosis of 30 fetuses at risk for fragile X syndrome
1 2
1459 10 14 1488 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):362-364
Fisch GS; Carpenter N; HowardPeebles PN; Maddalena A; Simensen R; et al.
Lack of association between mutation size and cognitive/behavior deficits in fragile X males: A brief report
1 3
1460 3 18 1494 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):395-398
Piussan C; Mathieu M; Berquin P; Fryns JP
Fragile X mutation and FG syndrome-like phenotype
1 4
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
1461 14 19 1495 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):404-407
Kambouris M; Snow K; Thibodeau S; Bluhm D; Green M; et al.
Segregation of the fragile X mutation from a male with a full mutation: Unusual somatic instability in the FMR-1 locus
1 3
1462 10 25 1505 1996 ANNALS OF CLINICAL AND LABORATORY SCIENCE 26(4):323-328
Mark HFL; Bier JAB; Scola P
The frequency of chromosomal abnormalities in patients referred for fragile X analysis
1 4
1463 4 13 1509 1996 ARCHIVES OF MEDICAL RESEARCH 27(4):587-588
Rivera H
Fragile X studies and authorship
1 5
1464 64 95 1517 1996 CHILD AND ADOLESCENT PSYCHIATRIC CLINICS OF NORTH AMERICA 5(4):895-&
Hagerman RJ
Fragile X syndrome
1 9
1465 11 21 1522 1996 CLINICAL OBSTETRICS AND GYNECOLOGY 39(4):772-782
Finucane B
Should all pregnant women be offered carrier testing for fragile X syndrome?
1 1
1466 1 4 1557 1996 JOURNAL OF SLEEP RESEARCH 5(4):272-272
Musumeci SA; Ferri R; Elia M; DelGracco S; Scuderi C; et al.
Normal respiratory pattern during sleep in young fragile X-syndrome patients
1 1
1467 3 45 1560 1996 MEDICAL ANTHROPOLOGY QUARTERLY 10(4):537-550
Nelkin D
The social dynamics of genetic testing: The case of Fragile-X
1 6
1468 4 138 1561 1996 MEDICAL HYPOTHESES 47(4):289-298
Fischer KM
Genes for Prader Willi Syndrome Angelman syndrome and fragile X syndrome are homologous, with genetic imprinting and unstable trinucleotide repeats causing mental retardation, autism and aggression
1 4
1469 16 28 1572 1996 PSYCHIATRIC GENETICS 6(2):81-86
Ashworth A; Abusaad I; Walsh C; Nanko S; Murray RM; et al.
Linkage analysis of the fragile X gene FMR-1 and schizophrenia: No evidence for linkage but report of a family with schizophrenia and an unstable triplet repeat
1 3
1470 8 27 1573 1996 PSYCHIATRY RESEARCH 64(2):97-104
Thompson NM; Rogeness GA; McClure E; Clayton R; Johnson C
Influence of depression on cognitive functioning in Fragile X females
1 6
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
1471 0 0 1594 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A30-A30
Gunter C; Paradee W; Newman J; Sherman SL; Warren ST
A novel biallelic polymorphism in the FMR1 gene shows strong linkage disequilibrium With CGG repeats and flanking microsatellite markers.
1 1
1472 0 0 1610 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A306-A306
Chiurazzi P; Pomponi MG; Willemsen R; Oostra BA; Neri G
In vitro reactivation of the fragile X syndrome gene.
1 1
1473 0 0 1612 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A316-A316
Nolin SL; Houck GE; Blumstein H; Ye LL; Dobkin CS; et al.
Single cell analysis shows different FMR1 CGG repeat stability in sperm and lymphocytes of premutation males.
1 2
1474 0 0 1613 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A321-A321
Tassone F; Hagerman RJ; Ikle D; Dyer PN; Lampe M; et al.
FMRP expression as a potential prognostic indicator in fragile X syndrome.
1 1
1475 4 11 1642 1997 BRITISH MEDICAL JOURNAL 315(7117):1174-1175
Barnicoat A
Screening for fragile X syndrome: a model for genetic disorders?
1 4
1476 10 16 1651 1997 DIAGNOSTIC MOLECULAR PATHOLOGY 6(3):161-166
Marini T; Pflueger S; Jackson A; Naber S; Karpells S; et al.
A five-year experience with fragile X testing - Setting laboratory standards of practice and a cost-effective protocol
1 2
1477 13 28 1653 1997 EUROPEAN JOURNAL OF HUMAN GENETICS 5(2):89-93
FulchignoniLataud MC; Olchwang S; Serre JL
The fragile X CGG repeat shows a marked level of instability in hereditary non-polyposis colorectal cancer patients
1 6
1478 6 15 1656 1997 GENETIC COUNSELING 8(1):1-6
Patsalis PC; Sismani C; Hadjimarcou MI; Rose N; Stylianidou G; et al.
Cytogenetic and fragile X molecular testing of individuals with mental retardation of unknown etiology
1 3
1479 1 2 1683 1997 JOURNAL OF MEDICAL GENETICS 34(4):350-350
Loesch DZ
FMR1 fully expanded mutation with minimal methylation in a high functioning fragile X male
1 1
1480 11 15 1687 1997 JOURNAL OF MEDICAL GENETICS 34(11):924-926
Losekoot M; Hoogendoorn E; Olmer R; Jansen CCAM; Oosterwijk JC; et al.
Prenatal diagnosis of the fragile X syndrome: loss of mutation owing to a double recombinant or gene conversion event at the FMR1 locus
1 7
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
1481 1 1 1697 1997 NATURE STRUCTURAL BIOLOGY 4(10):840-840
Musco G; Kharrat A; Stier G; Fraternali F; Gibson TJ; et al.
The solution structure of the first KH domain of FMR1, the protein responsible for the fragile X syndrome (vol 4, pg 712, 1997)
1 2
1482 23 44 1706 1997 PSYCHIATRIC GENETICS 7(3):115-119
ODwyer J; Holmes J; Mueller R; Taylor G
The prevalence of Fragile-X syndrome in an institution for people with learning disability
1 3
1483 31 49 1708 1997 REVISTA DE NEUROLOGIA 25(143):1068-1071
EstevezGonzalez A; Roig C; Piles S; Pineda M; GarciaSanchez C
Fragile-X syndrome and mental retardation
1 1
1484 20 30 1720 1998 ANNALS OF HUMAN GENETICS 62:337-347
Huggins RM; Loesch DZ; Sherman SL
A branching non-linear autoregressive model for the transmission of the fragile X dynamic repeat mutation
1 2
1485 31 107 1731 1998 CURRENT OPINION IN GENETICS & DEVELOPMENT 8(2):245-253
Tapscott SJ; Klesert TR; Widrow RJ; Stoger R; Laird CD
Fragile-X syndrome and myotonic dystrophy: parallels and paradoxes
1 10
1486 12 14 1732 1998 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 40(1):62-64
Gringras P; Barnicoat A
Retesting for fragile X syndrome in cytogenetically normal males
1 3
1487 4 7 1747 1998 HUMAN GENETICS 102(1):54-56
Storm K; Handig I; Reyniers E; Oostra BA; Kooy RF; et al.
Incomplete EcoRI digestion may lead to false diagnosis of fragile X syndrome
1 1
1488 17 40 1784 1998 JOURNAL OF NEUROSCIENCE RESEARCH 51(1):41-48
Berry-Kravis E; Ciurlionis R
Overexpression of fragile X gene (FMR-1) transcripts increases cAMP production in neural cells
1 1
1489 30 41 1795 1998 REVISTA MEDICA DE CHILE 126(8):911-918
Jara L; Lopez M; Mellado C; Aspillaga M; Avendano I; et al.
Clinical and metabolic screening for fragile X syndrome in 300 patients with unspecific mental retardation
1 1
1490 10 25 1796 1998 REVISTA MEDICA DE CHILE 126(12):1447-1454
Aspillaga M; Jara L; Avendano I; Lopez M
Fragile X syndrome. Clinical analysis of 300 Chilean patients with unspecific mental retardation
1 1
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
1491 38 61 1824 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):221-236
Holden JJA; Percy M; Allingham-Hawkins D; Brown WT; Chiurazzi P; et al.
Eighth International Workshop on the Fragile X Syndrome and X-linked Mental Retardation, August 16-22, 1997
1 4
1492 13 22 1852 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):217-220
Patsalis PC; Sismani C; Stylianou S; Ioannou P; Joseph G; et al.
Genetic variation and intergenerational FMR1 CGG-repeat stability in 100 unrelated three-generation families from the normal population
1 2
1493 18 22 1855 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):229-232
Petek E; Kroisel PM; Schuster M; Zierler H; Wagner K
Mosaicism in a fragile X male including a de novo deletion in the FMR1 gene
1 1
1494 5 13 1864 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 85(3):197-201
Freedenberg DL; Gane LW; Richards CS; Lampe M; Hills J; et al.
Fragile X syndrome and an isodicentric X chromosome in a woman with multiple anomalies, developmental delay, and normal pubertal development
1 1
1495 10 14 1865 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 85(3):311-316
Grasso M; Faravelli F; Lo Nigro C; Chiurazzi P; Sperandeo MP; et al.
Mosaicism for the full mutation and a microdeletion involving the CGG repeat and flanking sequences in the FMR1 gene in eight fragile X patients
1 1
1496 7 12 1866 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 86(2):162-164
Sun YJ; Baumer A
Nonrandom X inactivation and selection of fragile X full mutation in fetal fibroblasts
1 3
1497 17 24 1870 1999 AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY 181(4):789-792
Wenstrom KD; Descartes M; Franklin J; Cliver SP
A five-year experience with fragile X screening of high-risk gravid women
1 1
1498 0 0 1873 1999 ARCHIVES OF CLINICAL NEUROPSYCHOLOGY 14(8):767-768
Lanham DC; Mazzocco MM; Denckla MB
Depression and anxiety in girls with Fragile X or Turner Syndrome.
1 1
1499 15 19 1878 1999 CLINICAL CHEMISTRY AND LABORATORY MEDICINE 37(4):397-401
Houdayer C; Lemonnier A; Gerard M; Chauve C; Tredano M; et al.
Improved fluorescent PCR-based assay for sizing CGG repeats at the FRAXA locus
1 6
1500 6 14 1896 1999 GENETICS AND MOLECULAR BIOLOGY 22(4):471-474
Vianna-Morgante AM; Costa SS; Pavanello RDM; Otto PA; Mingroni-Netto RC
Premature ovarian failure (POF) in Brazilian fragile X carriers
1 4

#	LCR	NCR	Nodes / Date / Journal / Authors	LCS	GCS
1201	3	26	1278 1994 NUCLEIC ACIDS RESEARCH 22(9):1735-1740 HAN J; HSU CC; ZHU Z; LONGSHORE JW; FINLEY WH OVER-REPRESENTATION OF THE DISEASE-ASSOCIATED (CAG) AND (CGG) REPEATS IN THE HUMAN GENOME	2	25
1202	0	0	1292 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):153-153 BLACK SH; LEVINSON G; HARTON GL; PALMER FT; SISSON ME; et al. PREIMPLANTATION GENETIC TESTING (PGT) FOR FRAGILE-X (FRAX)	2	3
1203	11	13	1325 1995 AMERICAN JOURNAL OF MEDICAL GENETICS 55(3):384-386 PRIOR TW; PAPP AC; SNYDER PJ; SEDRA MS; GUIDA M; et al. GERMLINE MOSAICISM AT THE FRAGILE-X LOCUS	2	7
1204	2	5	1326 1995 AMERICAN JOURNAL OF MEDICAL GENETICS 57(3):508-509 LAXOVA R FRAGILE-X SCREENING - WHAT IS THE REAL ISSUE	2	3
1205	18	19	1331 1995 AMERICAN JOURNAL OF MEDICAL GENETICS 60(4):302-306 MUELLER OT; HARTSFIELD JK; AMAR MJA; GALLARDO LA; KOUSSEFF BG FRAGILE-X SYNDROME - DISCORDANT LEVELS OF CGG REPEAT MOSAICISM IN 2 BROTHERS	2	5
1206	27	43	1336 1995 ARCHIVES OF DISEASE IN CHILDHOOD 72(1):3-5 TURK J FRAGILE-X SYNDROME	2	4
1207	11	19	1339 1995 ARCHIVES OF MEDICAL RESEARCH 26:S77-S83 DiazGallardo MY; BarrosNunez P; Diaz CA; Hernandez A; GomezEspinel I; et al. Molecular characterization of the fragile-X syndrome in the Mexican population	2	4
1208	40	112	1342 1995 BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE 1271(2-3):293-303 FLANNERY AV; HIRST MC; KNIGHT SJL; RITCHIE RJ; DAVIES KE THE FRAGILE-X SYNDROME	2	5
1209	0	1	1353 1995 BRITISH MEDICAL JOURNAL 310(6973):148-148 CRAFT N STUDY SUPPORTS SCREENING FOR THE FRAGILE-X-SYNDROME	2	3
1210	45	78	1355 1995 CLINICS IN LABORATORY MEDICINE 15(4):859-& Brown WT Perspectives and molecular diagnosis of the fragile X syndrome	2	2
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1211	32	75	1359 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):187-198 Abrams MT; Reiss AL Quantitative brain imaging studies of fragile X syndrome	2	3
1212	3	16	1361 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):218-222 Musumeci SA; Ferri R; Elia M; DalGracco S; Scuderi C; et al. Sleep neurophysiology in fragile X patients	2	3
1213	5	9	1380 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):408-410 HowardPeebles PN; Maddalena A; Black SH; Levinson G; Bick DP; et al. Fragile X screening in pediatric and obstetrical patients	2	2
1214	1	4	1391 1995 GENETIC COUNSELING 6(4):293-296 FRYNS JP SCREENING FOR THE FRAGILE-X SYNDROME - THE NECESSITY OF INTERNATIONAL GUIDELINES FOR MOLECULAR-GENETICS PREDICTIVE TESTING IN GENERAL	2	3
1215	17	33	1393 1995 HUMAN GENETICS 96(3):323-329 DREESEN JCFM; GERAEDTS JPM; DUMOULIN JCM; EVERS JLH; PIETERS MHEC RS46(DXS548) GENOTYPING OF REPRODUCTIVE CELLS - APPROACHING PREIMPLANTATION TESTING OF THE FRAGILE-X SYNDROME	2	7
1216	2	14	1409 1995 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 39:326-330 SIMON EW; RAPPAPORT DA; PAPKA M; WOODRUFFPAK DS FRAGILE-X AND DOWNS-SYNDROME - ARE THERE SYNDROME-SPECIFIC COGNITIVE PROFILES AT LOW IQ LEVELS	2	4
1217	0	0	1411 1995 JOURNAL OF MEDICAL GENETICS 32(2):144-145 MORTON JE; RINDL PM; BULLOCK S; BUNDEY S; WEBB T FRAGILE-X SYNDROME IS LESS COMMON THAN PREVIOUSLY ESTIMATED	2	2
1218	8	12	1418 1995 JOURNAL OF MEDICAL GENETICS 32(11):907-908 PINTADO E; DEDIEGO Y; HMADCHA A; CARRASCO M; SIERRA J; et al. INSTABILITY OF THE CGG REPEAT AT THE FRAXA LOCUS AND VARIABLE PHENOTYPIC-EXPRESSION IN A LARGE FRAGILE-X PEDIGREE	2	9
1219	23	35	1436 1995 PRENATAL DIAGNOSIS 15(9):801-807 CASTELLVIBEL S; MILA M; SOLER A; CARRIO A; SANCHEZ A; et al. PRENATAL-DIAGNOSIS OF FRAGILE-X SYNDROME - (CGG)(N) EXPANSION AND METHYLATION OF CHORIONIC VILLUS SAMPLES	2	6
1220	15	34	1448 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):1-14 Tranebjaerg L; Lubs HA; Borghgraef M; Brown WT; Fisch G; et al. Seventh International Workshop on the Fragile X and X-linked Mental Retardation	2	4
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1221	4	6	1492 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):377-377 HowardPeebles PN Successful pregnancy in a fragile X carrier by donor egg	2	3
1222	13	56	1524 1996 COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY 61:689-697 Liu Q; Siomi H; Siomi MC; Fischer U; Zhang Y; et al. Molecular characterization of the protein products of the fragile X syndrome gene and the survival of motor neurons gene	2	10
1223	7	55	1537 1996 HUMAN GENETICS 98(2):151-157 Kramer PR; Pearson CE; Sinden RR Stability of triplet repeats of myotonic dystrophy and fragile X loci in human mutator mismatch repair cell lines	2	27
1224	28	77	1575 1996 SCREENING 4(4):175-192 Meadows KL; Sherman SL Fragile X syndrome: Examination of issues pertaining to population-based screening	2	2
1225	8	13	1624 1997 AMERICAN JOURNAL OF MEDICAL GENETICS 72(2):245-246 Healey SC; Duffy DL; Martin NG; Turner G Is fragile X syndrome a risk factor for dizygotic twinning?	2	4
1226	13	51	1626 1997 AMERICAN JOURNAL OF MEDICAL GENETICS 73(4):463-469 Ritchie RJ; Chakrabarti L; Knight SJL; Harding RM; Davies KE Population genetics of the FRAXE and FRAXF GCC repeats, and a novel CGG repeat, in Xq28	2	6
1227	27	35	1640 1997 BRAZILIAN JOURNAL OF GENETICS 20(4):731-739 Mingroni-Netto RC; Pavanello RCM; Otto PA; Vianna-Morgante AM Experience with molecular and cytogenetic diagnosis of fragile X syndrome in Brazilian families	2	2
1228	42	64	1648 1997 CURRENT OPINION IN NEUROLOGY 10(2):142-147 Chakrabarti L; Davies KE Fragile X syndrome	2	4
1229	11	19	1657 1997 GENETIC TESTING 1(3):151-155 Das S; Kubota T; Song M; Daniel R; Berry-Kravis EM; et al. Methylation analysis of the fragile X syndrome by PCR	2	3
1230	10	16	1663 1997 HUMAN GENETICS 101(2):186-189 Pesso R; Barkai G; Ravia Y; Gak E; Frydman M; et al. No founder effect detected in Jewish Ashkenazi patients with fragile-X syndrome	2	4
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1231	5	12	1690 1997 JOURNAL OF SPECIAL EDUCATION 31(3):362-376 Powell L; Houghton S; Douglas G Comparison of etiology-specific cognitive functioning profiles for individuals with fragile X and individuals with Down syndrome	2	4
1232	8	35	1691 1997 JOURNAL OF THEORETICAL BIOLOGY 188(1):53-67 Bat O; Kimmel M; Axelrod DE Computer simulation of expansions of DNA triplet repeats in the fragile X syndrome and Huntington's disease	2	4
1233	4	10	1709 1997 SOUTH AFRICAN MEDICAL JOURNAL 87(4):418-420 Goldman A; Krause A; Jenkins T Fragile X syndrome occurs in the South African black population	2	4
1234	12	28	1726 1998 CLINICAL GENETICS 53(3):179-183 Chan SY; Wong V DNA diagnosis of FRAXA and FRAXE in Chinese children with neurodevelopmental disorders and fragile X syndrome	2	5
1235	23	30	1741 1998 EUROPEAN JOURNAL OF HUMAN GENETICS 6(5):518-522 Peixoto A; dos Santos MR; Seruca R; Amorim A; Castedo S Analysis of FMR1 and flanking microsatellite markers in normal and fragile X chromosomes in Portugal: evidence for a "protector" haplotype	2	2
1236	0	0	1813 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A269-A269 DiMarco SP; Ceman S; Torre E; Warren ST FMRP is a phosphoprotein and a substrate of the Fes non-receptor tryosine kinase.	2	3
1237	5	20	1822 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 82(3):206-211 McConkie-Rosell A; Spiridigliozzi GA; Rounds K; Dawson DV; Sullivan JA; et al. Parental attitudes regarding carrier testing in children at risk for fragile X syndrome	2	7
1238	4	9	1829 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):281-285 Teisl JT; Reiss AL; Mazzocco MMM Maximizing the sensitivity of a screening questionnaire for determining fragile X at-risk status	2	2
1239	4	28	1832 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):298-301 Kotilainen J; Pirinen S Dental maturity is advanced in fragile X syndrome	2	2
1240	19	35	1833 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):302-307 Parvari R; Mumm S; Galil A; Manor E; Bar-David Y; et al. Deletion of 8.5 Mb, including the FMR1 gene, in a male with the fragile X syndrome phenotype and overgrowth	2	6
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1241	6	11	1841 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):338-341 Dobkin C; Ding XH; Li SY; Houck G; Nolin SL; et al. Accelerated prenatal diagnosis of fragile X syndrome by polymerase chain reaction restriction fragment detection	2	3
1242	8	14	1842 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):342-346 Jenkins EC; Wen GY; Kim KS; Zhong N; Sapienza VJ; et al. Prenatal fragile X detection using cytoplasmic and nuclear-specific monoclonal antibodies	2	2
1243	21	26	1850 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):204-207 Mingroni-Netto RC; Costa SS; Angeli CB; Vianna-Morgante AM DXS548/FRAXAC1 haplotypes in fragile X chromosomes in the Brazilian population	2	6
1244	10	14	1851 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):214-216 Pekarik V; Blazkova M; Kozak L Haplotype analysis of the fragile X syndrome gene FMR1 in the Czech Republic	2	5
1245	4	11	1862 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):306-308 Syrrou M; Georgiou I; Patsalis PC; Bouba I; Adonakis G; et al. Fragile X premutations and (TA)n estrogen receptor polymorphism in women with ovarian dysfunction	2	11
1246	34	44	1879 1999 CLINICAL GENETICS 55(5):346-351 Tassone F; Longshore J; Zunich J; Steinbach P; Salat U; et al. Tissue-specific methylation differences in a fragile X premutation carrier	2	4
1247	8	12	1880 1999 CLINICAL GENETICS 56(1):98-99 Millan JM; Martinez F; Cadroy A; Gandia J; Casquero M; et al. Screening for FMR1 mutations among the mentally retarded: prevalence of the fragile X syndrome in Spain	2	3
1248	35	50	1882 1999 CURRENT OPINION IN PSYCHIATRY 12(5):573-578 Harris SW; Hagerman RJ Fragile X syndrome: new developments	2	2
1249	19	34	1911 1999 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 43:314-324 York A; von Fraunhofer N; Turk J; Sedgwick P Fragile-X syndrome, Down's syndrome and autism: awareness and knowledge amongst special educators	2	4
1250	1	1	1930 1999 NATURE GENETICS 22(2):209-209 Coffee B Acetylated histones are associated with FMR1 in normal but not fragile X-syndrome cells (vol 22, pg 98, 1999)	2	5
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1251	14	23	1932 1999 PRENATAL DIAGNOSIS 19(13):1223-1230 Sermon K; Seneca S; Vanderfaeillie A; Lissens W; Joris H; et al. Preimplantation diagnosis for fragile X syndrome based on the detection of the non-expanded paternal and maternal CGG	2	26
1252	3	3	1941 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(1):256-258 Hundscheid RDL; Thomas CMG; Braat DDM; Oostra BA; Smits APT Premature ovarian failure is associated with maternally and paternally inherited premutation in Brazilian families with fragile X - Reply	2	5
1253	8	22	1968 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 92(5):336-342 McConkie-Rosell A; Spiridigliozzi GA; Sullivan JA; Dawson DV; Lachiewicz AM Carrier testing in fragile X syndrome: Effect on self-concept	2	4
1254	16	33	1973 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 95(2):123-129 Hjalgrim H; Hansen BF; Brondum-Nielsen K; Nolting D; Kjaer I Aspects of skeletal development in fragile X syndrome fetuses	2	4
1255	4	9	1977 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 95(5):516-517 Limprasert P; Jaruratanasirikul S; Vasiknanonte P Unilateral macroorchidism in fragile X syndrome	2	2
1256	33	48	1979 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 97(3):183-188 Willemsen R; Oostra BA FMRP detection assay for the diagnosis of the fragile X syndrome	2	4
1257	14	37	1982 2000 AMERICAN JOURNAL ON MENTAL RETARDATION 105(4):286-299 Kau ASM; Reider EE; Payne L; Meyer WA; Freund L Early behavior signs of psychiatric phenotypes in fragile X syndrome	2	4
1258	22	37	1983 2000 ANNALES DE GENETIQUE 43(1):29-34 Gonzalez-del Angel A; Vidal S; Saldana Y; del Castillo V; Alcantara MA; et al. Molecular diagnosis of the fragile X and FRAXE syndromes in patients with mental retardation of unknown cause in Mexico	2	4
1259	9	19	1988 2000 BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 275(2):608-610 Beaulieu MA A distinct FMRP polysomal population at an advanced stage of mammalian erythropoiesis	2	2
1260	1	6	2003 2000 CYTOGENETICS AND CELL GENETICS 89(1-2):11-13 Bardoni B; Giglio S; Schenck A; Rocchi M; Mandel JL Assignment of NUFIP1 (Nuclear FMRP Interacting Protein 1) gene to chromosome 13q14 and assignment of a pseudogene to chromosome 6q12	2	2
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1261	8	16	2040 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:81-85 Sabaratnam M Pathological and neuropathological findings in two males with fragile-X syndrome	2	4
1262	22	29	2072 2000 MENTAL RETARDATION 38(3):207-215 Maes B; Fryns JP; Ghesquiere P; Borghgraef M Phenotypic checklist to screen for fragile X syndrome in people with mental retardation	2	5
1263	6	14	2081 2000 NEUROBIOLOGY OF LEARNING AND MEMORY 74(1):80-93 Irwin SA; Swain RA; Christmon CA; Chakravarti A; Weiler IJ; et al. Evidence for altered fragile-x mental retardation protein expression in response to behavioral stimulation (vol 73, pg 87, 2000)	2	2
1264	6	26	2111 2001 AMERICAN JOURNAL OF MEDICAL GENETICS 98(1):37-45 McConkie-Rosell A; Spiridigliozzi GA; Sullivan JA; Dawson DV; Lachiewicz AM Longitudinal study of the carrier testing process for fragile X syndrome: Perceptions and coping	2	3
1265	27	32	2125 2001 ANNALS OF CLINICAL BIOCHEMISTRY 38:264-271 Saha S; Karmakar P; Chatterjee C; Banerjee D; Das S; et al. Fragile X syndrome in Calcutta, India	2	4
1266	35	47	2155 2001 HUMAN GENETICS 108(6):450-458 Weinhausel A; Haas OA Evaluation of the fragile X (FRAXA) syndrome with methylation-sensitive PCR	2	6
1267	11	91	2173 2001 JOURNAL OF LEARNING DISABILITIES 34(6):520-533 Mazzocco MMM Math learning disability and math LD subtypes: Evidence from studies of Turner syndrome, fragile X syndrome, and neurofibromatosis type 1	2	8
1268	15	47	2179 2001 JOURNAL OF SPECIAL EDUCATION 34(4):194-202 Symons FJ; Clark RD; Roberts JP; Bailey DB Classroom behavior of elementary school-age boys with fragile X syndrome	2	3
1269	13	30	2200 2001 REVISTA DE NEUROLOGIA 33:S24-S29 Cornish K; Munir F; Wilding J A neuropsychological and behavioural profile of a attention deficits in fragile X syndrome	2	2
1270	0	0	2218 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):185-185 Jacquemont S; Hagerman RJ; Leehey M; Greco C; Brunberg J; et al. Characterization of a progressive neurological condition in older adult male carriers of the fragile X premutation.	2	2
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1271	5	9	2252 2002 BRAIN & DEVELOPMENT 24(8):766-769 Incorpora G; Sorge G; Sorge A; Pavone L Epilepsy in fragile X syndrome	2	3
1272	7	21	2254 2002 CELLULAR & MOLECULAR BIOLOGY LETTERS 7(3):877-883 Denman RB Methylation of the arginine-glycine-rich region in the fragile X mental retardation protein FMRP differentially affects RNA binding	2	6
1273	66	84	2260 2002 CYTOGENETIC AND GENOME RESEARCH 99(1-4):257-264 Oostra BA; Willemsen R The X chromosome and fragile X mental retardation	2	3
1274	42	139	2262 2002 DEVELOPMENTAL PSYCHOBIOLOGY 40(3):323-338 Churchill JD; Grossman AW; Irwin SA; Galvez R; Klintsova AY; et al. A converging-methods approach to fragile X syndrome	2	8
1275	22	46	2286 2002 GENOMICS 80(4):423-432 Peier AM; Nelson DL Instability of a premutation-sized CGG repeat in FMR1 YAC transgenic mice	2	3
1276	17	39	2291 2002 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 32(2):107-114 Fisch GS; Simensen RJ; Schroer RJ Longitudinal changes in cognitive and adaptive Behavior scores in children and adolescents with the fragile X mutation or autism	2	3
1277	6	29	2299 2002 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 46:328-339 Kuo AY; Reiss AL; Freund LS; Huffman LC Family environment and cognitive abilities in girls with fragile-X syndrome	2	3
1278	15	20	2310 2002 MICROSCOPY RESEARCH AND TECHNIQUE 57(3):145-147 Feng Y Fragile X mental retardation: Misregulation of protein synthesis in the developing brain?	2	2
1279	20	42	2313 2002 MICROSCOPY RESEARCH AND TECHNIQUE 57(3):159-167 Kates WR; Folley BS; Lanham DC; Capone GT; Kaufmann WE Cerebral growth in fragile X syndrome: Review and comparison with Down syndrome	2	6
1280	25	35	2315 2002 MICROSCOPY RESEARCH AND TECHNIQUE 57(3):174-178 Kau ASM; Meyer WA; Kaufmann WE Early development in males with fragile X syndrome: A review of the literature	2	3
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1281	24	59	2326 2002 NEUROBIOLOGY OF DISEASE 11(1):221-229 Castren M; Lampinen KE; Miettinen R; Koponen E; Sipola I; et al. BDNF regulates the expression of fragile X mental retardation protein mRNA in the hippocampus	2	4
1282	8	58	2335 2002 NUCLEIC ACIDS RESEARCH 30(17):3672-3681 Weisman-Shomer P; Cohen E; Fry M Distinct domains in the CArG-box binding factor A destabilize tetraplex forms of the fragile X expanded sequence d(CGG)(n)	2	3
1283	15	39	2385 2003 AMERICAN JOURNAL ON MENTAL RETARDATION 108(3):149-160 Abbeduto L; Murphy MM; Cawthon SW; Richmond EK; Weissman MD; et al. Receptive language skills of adolescents and young adults with Down or fragile X syndrome	2	5
1284	14	43	2398 2003 BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 310(1):1-7 Denman RB Deja vu all over again: FMRP binds U-rich target mRNAs	2	4
1285	20	38	2407 2003 BRAIN TOPOGRAPHY 15(3):165-171 Castren M; Paakkonen A; Tarkka IM; Ryynanen M; Partanen J Augmentation of auditory N1 in children with fragile X syndrome	2	2
1286	69	87	2411 2003 CURRENT OPINION IN PEDIATRICS 15(6):559-566 Chiurazzi P; Neri G; Oostra BA Understanding the biological underpinnings of fragile X syndrome	2	5
1287	28	62	2501 2004 BRAIN 127:591-601 Kogan CS; Boutet I; Cornish K; Zangenehpour S; Mullen KT; et al. Differential impact of the FMR1 gene on visual processing in fragile X syndrome	2	2
1288	16	47	2509 2004 CURRENT BIOLOGY 14(12):1025-1034 Xu KY; Bogert BA; Li WJ; Su K; Lee A; et al. The fragile X-related gene affects the crawling behavior of Drosophila larvae by regulating the mRNA level of the DEG/ENaC protein pickpocket1	2	3
1289	20	37	2510 2004 CURRENT BIOLOGY 14(20):1863-1870 Pan LY; Zhang YQ; Woodruff E; Broadie K The Drosophila fragile X gene negatively regulates neuronal elaboration and synaptic differentiation	2	2
1290	23	34	2561 2004 JOURNAL OF NEUROSCIENCE 24(33):7272-7276 Stefani G; Fraser CE; Darnell JC; Darnell RB Fragile X mental retardation protein is associated with translating polyribosomes in neuronal cells	2	3
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1291	42	102	2575 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):60-67 Willemsen R; Oostra BA; Bassell GJ; Dictenberg J The fragile X syndrome: From molecular genetics to neurobiology	2	5
1292	47	73	2590 2004 NATURE CELL BIOLOGY 6(11):1048-1053 Jin P; Alisch RS; Warren ST RNA and microRNAs in fragile X mental retardation	2	3
1293	24	40	2603 2004 NUCLEIC ACIDS RESEARCH 32(7):2129-2137 Gabus C; Mazroui R; Tremblay S; Khandjian EW; Darlix JL The fragile X mental retardation protein has nucleic acid chaperone properties	2	5
1294	0	0	10 1981 AMERICAN JOURNAL OF HUMAN GENETICS 33(6):A100-A100 CARPENTER NJ; LEICHTMAN LG; LOGAN A; SAY B FRAGILE X-LINKED MENTAL-RETARDATION	1	1
1295	0	0	11 1981 AMERICAN JOURNAL OF HUMAN GENETICS 33(6):A107-A107 HOWARDPEEBLES PN; FINLEY WH TESTICULAR AND CYTOGENETIC SCREENING OF RETARDED MALES FROM THE SOUTH FOR THE FRAGILE X-LINKED MENTAL-RETARDATION SYNDROME	1	1
1296	0	0	12 1981 AMERICAN JOURNAL OF HUMAN GENETICS 33(6):A122-A122 SHAPIRO LR; KUHR MD; WILMOT PL; LILIENTHAL ER; HIGGS LC MULTIPLE SIBLING MENTAL-RETARDATION AND THE IMPACT OF THE FRAGILE X-CHROMOSOME	1	1
1297	0	0	15 1981 CANADIAN JOURNAL OF NEUROLOGICAL SCIENCES 8(2):191-191 SERGOVICH F; POZSONYI J; HINTON G RECENT ADVANCES IN MENTAL-RETARDATION THE FRAGILE X-CHROMOSOME	1	0
1298	0	2	17 1981 CLINICAL GENETICS 19(2):140-141 SOUDEK D; GORZNY N NO FRAGILE X-CHROMOSOME IN NORMAL MEN	1	3
1299	0	0	18 1981 CLINICAL GENETICS 19(6):493-493 NIELSEN KB; TOMMERUP N; POULSEN H; MIKKELSEN M DANISH FAMILIES WITH X-LINKED MENTAL-RETARDATION AND FRAGILE X-CHROMOSOME	1	1
1300	0	0	35 1981 PEDIATRIC RESEARCH 15(4):569-569 SHAPIRO LR; KUHR MD; WILMOT PL MULTIPLE SIBLING MENTAL-RETARDATION AND THE IMPACT OF THE FRAGILE X-CHROMOSOME	1	1
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1301	0	0	36 1981 PEDIATRIC RESEARCH 15(4):645-645 PUESCHEL SM; HAYS R; MENDOZA T A FAMILIAL X-LINKED MENTAL-RETARDATION SYNDROME ASSOCIATED WITH MULTIPLE CONGENITAL-ANOMALIES, MEGALOGENITALIA AND A FRAGILE X-CHROMOSOME	1	1
1302	0	0	42 1982 AMERICAN JOURNAL OF HUMAN GENETICS 34(6):A93-A93 HAVKIN S; CHAKI R; GOLDMAN B FRAGILE X-CHROMOSOME IN 2 FAMILIES WITH X-LINKED MENTAL-RETARDATION	1	1
1303	0	0	43 1982 AMERICAN JOURNAL OF HUMAN GENETICS 34(6):A103-A103 NOLIN S; BROWN T; JENKINS E FRAGILE-X SYNDROME - DILEMMAS FOR GENETIC-COUNSELING	1	1
1304	0	0	45 1982 AMERICAN JOURNAL OF HUMAN GENETICS 34(6):A121-A121 CHUDLEY AE; KNOLL J; GERRARD JW; SHEPEL L; MCGAHEY E; et al. FRAGILE X-LINKED MENTAL-RETARDATION - EFFECT OF AGE AND INTELLIGENCE ON EXPRESSION OF FRAGILE-X	1	1
1305	0	0	48 1982 AMERICAN JOURNAL OF HUMAN GENETICS 34(6):A131-A131 KNOLL J; CHUDLEY AE; GERRARD JW EFFICACY OF FUDR IN ENHANCING EXPRESSION OF FRA(X) IN AFFECTED MALES AND CARRIER FEMALES WITH FRAGILE X-LINKED MENTAL-RETARDATION	1	1
1306	0	0	57 1982 CLINICAL RESEARCH 30(2):A292-A292 JENKINS EC; BROWN WT; DUNCAN CJ; BROOKS J DEMONSTRATION OF THE FRAGILE X-CHROMOSOME IN AMNIOTIC-FLUID CELLS	1	2
1307	0	0	59 1982 CLINICAL RESEARCH 30(5):A891-A891 MIXON C; DEV V EFFECT OF FUDR AND METHIONINE ON THE EXPRESSION OF FRAGILE X IN A LYMPHOBLASTOID CELL-LINE	1	1
1308	0	0	60 1982 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 24(2):252-253 SERGOVICH F; POZSONYI J; HINTON GG RECENT ADVANCES IN MENTAL-RETARDATION - THE FRAGILE X-CHROMOSOME	1	1
1309	1	5	61 1982 HOSPITAL PRACTICE 17(7):17-& BROWN WT; JENKINS EC FRAGILE X - ITS DETECTABILITY	1	1
1310	0	0	85 1982 PEDIATRICS 69(5):669-669 GERALD PS X-LINKED MENTAL-RETARDATION AND FRAGILE-X OR MARKER-X SYNDROME - REPLY	1	1
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1311	5	37	87 1982 WESTERN JOURNAL OF MEDICINE 137(4):278-281 MOORE BC; GLOVER TW; KAISERMCCAW B; HECHT F FRAGILE X-LINKED MENTAL-RETARDATION AND MACRO-ORCHIDISM	1	3
1312	0	21	88 1982 WIENER KLINISCHE WOCHENSCHRIFT 94(8):217-219 FONATSCH C; FLATZ SD FRAGILE X-CHROMOSOME AND X-LINKED MENTAL-RETARDATION	1	1
1313	0	0	102 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A146-A146 OBRIEN MM; PADREMENDOZA T; PUESCHEL SM MATERNAL NONDISJUNCTION OF FRAGILE X-CHROMOSOME RESULTING IN KLINEFELTER SYNDROME	1	2
1314	1	1	110 1983 AMERICAN JOURNAL OF MEDICAL GENETICS 14(4):797-797 HECHT F; JACKY PB; SUTHERLAND GR FRAGILE X-CHROMOSOME IN NORMAL MALES - REPLY	1	2
1315	2	15	115 1983 ANNALES DE GENETIQUE 26(3):171-173 JACKY PB; DILL FJ FRAGILE-X CHROMOSOME AND CHROMOSOME CONDENSATION	1	4
1316	0	0	123 1983 CLINICAL GENETICS 23(3):236-236 PAJARES IL; DELICADO A; GALLEGO A; CASTROVIEJO IP FAMILIAL X-LINKED MENTAL-RETARDATION AND FRAGILE X-CHROMOSOMES IN 6 SPANISH FAMILIES	1	1
1317	0	0	124 1983 CLINICAL GENETICS 23(3):241-241 NIELSEN KB; TOMMERUP N; MIKKELSEN M CLINICAL AND CYTOGENETIC FINDINGS IN 26 MENTALLY-RETARDED MALES WITH THE FRAGILE-X	1	1
1318	0	0	125 1983 CLINICAL GENETICS 23(3):250-251 TEJADA I; NICOLAS H; CHERUY C; BOUE J STUDY OF A LARGE SIBSHIP WITH MENTALLY-RETARDED MALES AND FEMALES CARRYING FRAGILE-X	1	1
1319	8	28	142 1983 IRISH JOURNAL OF MEDICAL SCIENCE 152(12):440-445 DEARCE MA; LAW E; MASTERSON JG NON-SPECIFIC X-LINKED MENTAL-RETARDATION WITH FRAGILE-X CHROMOSOME - SOMATIC FEATURES, CYTOGENETIC DIAGNOSIS AND ELEMENTS FOR GENETIC-COUNSELING	1	3
1320	0	0	160 1983 PEDIATRIE 38(3):191-198 JALBERT P FRAGILE X-LINKED MENTAL-RETARDATION - MORE QUESTIONS	1	3
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1321	1	2	184 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):275-276 HOWARDPEEBLES PN; CARROLL AJ RECOMBINATION BETWEEN THE FRAGILE-X AND G6PD	1	3
1322	0	0	203 1984 EUROPEAN JOURNAL OF PEDIATRICS 141(4):265-265 LARGO RH; SCHINZEL A DEVELOPMENTAL AND BEHAVIORAL DISTURBANCES IN BOYS WITH THE FRAGILE-X SYNDROME	1	4
1323	0	1	205 1984 HUMAN GENETICS 66(1):100-100 GARDNER RJM FRAGILE-X HOMOZYGOSITY DUE TO SOMATIC CROSSING-OVER	1	2
1324	2	10	207 1984 HUMAN GENETICS 68(2):189-190 REIDY JA; CHEN ATL FOLIC-ACID AND CHROMOSOME BREAKAGE .2. A METHIONINE EFFECT SIMILAR TO THAT IN FRAGILE-X EXPRESSION	1	9
1325	2	6	214 1984 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 14(4):451-452 JACKSON A; HOGERMAN R; LEVITAS A SEROTONIN LEVELS IN FRAGILE-X AUTISTIC PATIENTS	1	3
1326	1	3	217 1984 JOURNAL OF MEDICAL GENETICS 21(1):74-75 SUTHERLAND GR ROUTINE DIAGNOSTIC-DETECTION OF THE FRAGILE X	1	4
1327	2	4	225 1984 LANCET 1(8370):220-220 JANCAR J PREVALENCE OF FRAGILE X-CHROMOSOME	1	3
1328	3	6	235 1984 PRENATAL DIAGNOSIS 4(6):473-474 VENTER PA; COETZEE DJ; BADENHORST A; MARX MP; HOF JO; et al. A CONFIRMED PRENATAL-DIAGNOSIS OF A FEMALE FETUS WITH THE FRAGILE X-CHROMOSOME	1	4
1329	4	12	250 1985 AMERICAN JOURNAL OF MEDICAL GENETICS 21(4):771-775 SHIMANUKI K; LIN MS; WILSON MG REDUCTION OF FRAGILE X-EXPRESSION IN BLOOD AFTER CRYOPRESERVATION	1	3
1330	7	13	251 1985 AMERICAN JOURNAL OF MEDICAL GENETICS 22(2):415-416 BARBI G; STEINBACH P FRAGILE-X AND MARTIN-BELL SYNDROME - NEW SOURCE OF INFORMATION	1	3
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1331	5	14	268 1985 CLINICAL GENETICS 27(6):529-534 WEBB TP CO-CULTIVATION STUDIES IN THE EXPRESSION OF FRAGILE(X) (Q27) IN LYMPHOCYTES	1	2
1332	3	6	270 1985 CLINICAL GENETICS 28(5):399-400 SOUDEK D DECREASE OF FRAGILE X-FREQUENCY IN STORED-BLOOD SAMPLES - INDIVIDUAL VARIABILITY	1	1
1333	0	4	278 1985 CYTOGENETICS AND CELL GENETICS 40(1-4):726-726 PURRELLO M; ALHADEFF B; ROCCHI M; ARCHIDIACONO N; DRAYNA D; et al. RELATIVE POSITIVE OF POLYMORPHIC DNA LOCI OF THE HUMAN X-CHROMOSOME LONG ARM SUBTELOMERIC REGION WITH RESPECT TO THE FRAGILE X SITE (FRAXQ27)	1	4
1334	3	5	291 1985 HUMAN GENETICS 71(2):182-182 PEMBREY ME; WINTER RM FURTHER SEGREGATION ANALYSIS OF THE FRAGILE X-SYNDROME WITH SPECIAL REFERENCE TO TRANSMITTING MALES	1	1
1335	2	3	292 1985 HUMAN GENETICS 71(2):183-183 SHERMAN SL; JACOBS PA; MORTON NE FURTHER SEGREGATION ANALYSIS OF THE FRAGILE X-SYNDROME WITH SPECIAL REFERENCE TO TRANSMITTING MALES - REPLY	1	1
1336	2	2	297 1985 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 6(5):322-322 KERBESHIAN J; BURD L; MARTSOLF JT THE MULTIPOTENTIAL OUTCOME OF FRAGILE X-SYNDROME	1	1
1337	1	4	316 1986 AMERICAN JOURNAL OF DISEASES OF CHILDREN 140(4):327-327 BOWERS EJ FRAGILE-X SYNDROME AND LEARNING-DISABILITIES	1	2
1338	1	7	317 1986 AMERICAN JOURNAL OF DISEASES OF CHILDREN 140(4):327-328 HAGERMAN RJ FRAGILE-X SYNDROME AND LEARNING-DISABILITIES - REPLY	1	1
1339	4	4	346 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):527-530 TOMMERUP N; HOLMGREN G; STEINBACH P FRAGILE-X - CARRIER DETECTION IN PREGNANCY	1	4
1340	4	18	348 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):537-544 NIELSEN KB SEX-CHROMOSOME ANEUPLOIDY IN FRAGILE-X CARRIERS	1	6
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1341	0	0	379 1986 CLINICAL GENETICS 29(5):462-462 GOONEWARDENA P; GUSTAVSON KH; HOLMGREN G; TOLUN A; CHOTAI J; et al. STUDIES ON FRAGILE X-MENTAL RETARDATION BY THE USE OF DNA PROBES	1	1
1342	2	4	380 1986 CLINICAL GENETICS 29(5):475-475 TOMMERUP N THE FRAGILE X-CHROMOSOME - PRENATAL-DIAGNOSIS	1	3
1343	0	0	409 1986 PEDIATRIC RESEARCH 20(4):A269-A269 MURPHY PD; WATSON MS; KIDD KK; BREG WR MOLECULAR APPROACHES TO CARRIER DETECTION AND PRENATAL-DIAGNOSIS OF THE FRAGILE-X SYNDROME (MCKUSICK NUMBER 30920)	1	2
1344	1	4	416 1987 AMERICAN JOURNAL OF DISEASES OF CHILDREN 141(6):601-601 BARTOLUCCI G; SZATMARI P POSSIBLE SIMILARITIES BETWEEN THE FRAGILE-X AND ASPERGERS SYNDROMES	1	2
1345	1	1	417 1987 AMERICAN JOURNAL OF DISEASES OF CHILDREN 141(6):601-602 HAGERMAN RJ POSSIBLE SIMILARITIES BETWEEN THE FRAGILE-X AND ASPERGERS SYNDROMES - REPLY	1	1
1346	1	4	436 1987 BRITISH MEDICAL JOURNAL 295(6603):922-922 MCKINLEY MJ; NICOLAIDES KH; KEARNEY LU; HERON O FRAGILE-X SYNDROME	1	3
1347	10	29	437 1987 CLINICAL CHEMISTRY 33(10):1726-1730 THIBODEAU SN USE OF RESTRICTION-FRAGMENT-LENGTH-POLYMORPHISM ANALYSIS FOR DETECTING CARRIERS OF FRAGILE-X SYNDROME	1	1
1348	12	23	443 1987 CYTOGENETICS AND CELL GENETICS 44(2-3):118-122 LIN MS; SHIMANUKI K; WILSON MG EXPRESSION OF FRAGILE-X IN HUMAN-MOUSE SOMATIC-CELL HYBRIDS	1	1
1349	0	0	444 1987 CYTOGENETICS AND CELL GENETICS 46(1-4):587-587 BROWN WT; WU Y; GROSS AC; CHAN CB; DOBKIN CS; et al. LINKAGE OF FLANKING PROBES IN 40 FRAGILE X-FAMILIES	1	7
1350	0	0	448 1987 CYTOGENETICS AND CELL GENETICS 46(1-4):688-689 SCHWARTZ C; PATTERSON M; DAVIES K; TRUNCA C; TRASK B; et al. THE USE OF DISTAL DELETIONS OF XQ TO ORDER LOCI BETWEEN FACTOR-IX AND THE FRAGILE-X SITE (XQ27.3)	1	2
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1351	6	9	452 1987 GENETIKA 23(3):504-509 SULEIMANOVA DG; KULESHOV NP SPONTANEOUS AND INDUCED CHROMOSOMAL INSTABILITY IN PATIENTS WITH FRAGILE X-CHROMOSOME, SUFFERING FROM X-LINKED MENTAL-RETARDATION	1	3
1352	0	0	478 1987 JOURNAL OF MEDICAL GENETICS 24(10):640-640 SENIOR J; KILPATRICK M; WEBB T COMPARATIVE LINKAGE STUDIES IN THE FRAGILE X-SYNDROME	1	1
1353	0	0	479 1987 JOURNAL OF MEDICAL GENETICS 24(10):641-641 HULTEN M; JOHANNISSON R MEIOSIS IN THE FRAGILE-X MENTAL-RETARDATION SYNDROME	1	1
1354	2	4	481 1987 JOURNAL OF MENTAL DEFICIENCY RESEARCH 31:81-85 COWIE VA; SINGH KR; WHEATER R; BIRD J THE FRAGILE-X SYNDROME IN TWIN SISTERS	1	1
1355	1	2	487 1987 LANCET 2(8554):329-329 VERLOES A; SACRE JP; GEUBELLE F SOTOS SYNDROME AND FRAGILE-X CHROMOSOMES	1	5
1356	0	1	489 1987 NEW ENGLAND JOURNAL OF MEDICINE 316(8):483-483 TURNER G THE FRAGILE X-CHROMOSOME - REPLY	1	1
1357	0	0	490 1987 NEW ENGLAND JOURNAL OF MEDICINE 316(8):483-483 HECHT F; HECHT BK THE FRAGILE X-CHROMOSOME	1	1
1358	4	4	491 1987 NEW ENGLAND JOURNAL OF MEDICINE 316(8):483-483 BURD L THE FRAGILE X-CHROMOSOME	1	1
1359	0	0	494 1987 PRACTITIONER 231(1431):910-& BUNDEY S THE FRAGILE X-SYNDROME	1	1
1360	0	0	498 1987 TERATOLOGY 36(3):453-453 SUZUKI Y; CHYO H; MATSUI A; SHIMOMURA C; FUNAHASI M CLINICAL-DIAGNOSIS OF FRAGILE-X SYNDROME	1	2
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1361	0	0	505 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):20-21 KEREM B; GOITEIN R; SCHAAP T THE DISTRIBUTION OF FRAGILE-X CHROMOSOMES IN AMNIOTIC CELLS CULTURED BY THE INSITU TECHNIQUE	1	1
1362	6	11	522 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):177-183 MILONE G; CONTI L; RIZZO R; SANFILIPPO S; SAMMITO V; et al. A DERMATOGLYPHIC STUDY OF A GROUP OF SICILIAN CHILDREN WITH FRAGILE-X SYNDROME	1	2
1363	1	3	524 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):201-205 BROWN WT; RUDELLI RD; WISNIEWSKI HM FRAGILE-X SYNDROME - NEUROPATHOLOGY CENTER	1	1
1364	2	8	527 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):231-236 SUTHERS GK; TURNER G; MULLEY JC CASE-REPORT - FRAGILE-X SYNDROME AND NEPHROGENIC DIABETES-INSIPIDUS	1	2
1365	1	7	539 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):443-450 NOLIN SL; JENKINS EC; BROWN WT; DOBKIN CS INSITU NICK TRANSLATION OF THE FRAGILE-X REGION	1	2
1366	17	31	576 1988 CLINICAL GENETICS 33(6):410-417 VEENEMA H; BEVERSTOCK GC; DEKONING T; PEARSON PL; VANDEKAMP JJP THE FRAGILE X-CHROMOSOME - AN EVALUATION OF THE RESULTS IN A ROUTINE CYTOGENETIC LABORATORY IN THE PERIOD 1981-1986	1	3
1367	7	32	580 1988 CYTOGENETICS AND CELL GENETICS 47(4):177-180 HORI T; TAKAHASHI E; TSUJI H; TSUJI S; MURATA M FRAGILE-X EXPRESSION IN THYMIDINE-PROTOTROPHIC AND AUXOTROPHIC HUMAN-MOUSE SOMATIC-CELL HYBRIDS UNDER LOW AND HIGH THYMIDYLATE STRESS CONDITIONS	1	3
1368	2	17	590 1988 HUMAN GENETICS 79(3):231-234 JOHANNISSON R; FROSTERISKENIUS U; SAADALLAH N; HULTEN MA SPERMATOGENESIS IN 2 PATIENTS WITH THE FRAGILE-X SYNDROME .2. 1ST MEIOSIS - LIGHT AND ELECTRON-MICROSCOPY	1	3
1369	10	48	592 1988 HUMAN GENETICS 79(4):341-346 VANDAMME B; LIEBAERS I; HENS L; BERNHEIM JL; ROOBOL C THE ROLE OF FLUORINATED PYRIMIDINE ANALOGS IN THE INDUCTION OF THE INVITRO EXPRESSION OF THE FRAGILE X-CHROMOSOME	1	1
1370	27	63	612 1988 QUARTERLY JOURNAL OF MEDICINE 69(258):755-763 FROSTERISKENIUS U; PATTERSON MN; BELL MV; BLOOMFIELD J; DAVIES KE MOLECULAR ANALYSIS OF THE FRAGILE-X SYNDROME	1	1
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1371	3	31	613 1988 SCHIZOPHRENIA RESEARCH 1(4):277-281 DELISI LE; REISS AL; WHITE BJ; GERSHON ES CYTOGENETIC STUDIES OF MALES WITH SCHIZOPHRENIA - SCREENING FOR THE FRAGILE X-CHROMOSOME AND OTHER CHROMOSOMAL-ABNORMALITIES	1	36
1372	0	0	615 1989 AMERICAN FAMILY PHYSICIAN 39(5):185-193 SIMENSEN RJ; ROGERS RC FRAGILE-X SYNDROME	1	1
1373	4	53	628 1989 AMERICAN ZOOLOGIST 29(2):569-591 LAIRD CD FROM POLYTENE CHROMOSOMES TO HUMAN EMBRYOLOGY - CONNECTIONS VIA THE HUMAN FRAGILE-X SYNDROME	1	3
1374	6	8	630 1989 ARCHIVES OF DISEASE IN CHILDHOOD 64(9):1223-1224 WINTER RM FRAGILE-X MENTAL-RETARDATION	1	3
1375	2	10	637 1989 CYTOGENETICS AND CELL GENETICS 50(2-3):172-173 SAUER SM; PHELAN MC; RICHER CL; SCHWARTZ CE PHYSICAL MAPPING OF PROBES PROXIMAL TO THE FRAGILE-X LOCUS (FRAX) CONFIRMS THE ORDER F9-DXS105 (CX55.7)-DXS98 (4D8)-FRAXA	1	1
1376	0	0	662 1989 NEUROLOGIC CLINICS 7(1):107-121 BROWN WT THE FRAGILE-X SYNDROME	1	1
1377	21	41	667 1989 PSYCHOLOGY IN THE SCHOOLS 26(4):380-389 SIMENSEN RJ; ROGERS RC SCHOOL-PSYCHOLOGY AND MEDICAL DIAGNOSIS - THE FRAGILE X-SYNDROME	1	1
1378	2	3	671 1989 ZEITSCHRIFT FUR KINDER-UND JUGENDPSYCHIATRIE UND PSYCHOTHERAPIE 17(2):85-90 BLANK R MAIN SYMPTOMS - DELAYED LANGUAGE-DEVELOPMENT AND BEHAVIOR PROBLEMS - 2 CASE-REPORTS ON THE FRAGILE-X SYNDROME	1	1
1379	30	39	672 1989 ZEITSCHRIFT FUR KINDER-UND JUGENDPSYCHIATRIE UND PSYCHOTHERAPIE 17(2):91-97 VONGONTARD A PSYCHOPATHOLOGY ASSOCIATED WITH THE FRAGILE-X SYNDROME	1	2
1380	0	0	673 1989 ZHURNAL NEVROPATOLOGII I PSIKHIATRII IMENI S S KORSAKOVA 89(8):101-105 BLYUMINA MG CLINICAL SIGNS OF OLIGOPHRENIA WITH FRAGILE X-CHROMOSOME IN PREPUBERTY AND POSTPUBERTY MALES	1	2
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1381	12	20	682 1990 AMERICAN JOURNAL OF HUMAN GENETICS 47(6):988-993 OHASHI H; KUWANO A; TSUKAHARA M; ARINAMI T; KAJII T REPLICATION PATTERNS OF THE FRAGILE-X IN HETEROZYGOUS CARRIERS - ANALYSIS BY A BRDURD ANTIBODY METHOD	1	2
1382	6	13	699 1990 BRITISH JOURNAL OF HOSPITAL MEDICINE 43(1):17-17 BUNDEY S FRAGILE-X SYNDROME	1	1
1383	6	12	706 1990 HUMAN GENETICS 84(2):216-217 BUTLER MG NO SIGNIFICANT RELATIONSHIP BETWEEN AGE AND FREQUENCY OF CHROMOSOME LESIONS IN MENTALLY-RETARDED INDIVIDUALS WITH OR WITHOUT THE FRAGILE X-SYNDROME	1	4
1384	1	4	720 1990 JOURNAL OF NEUROLOGY 237(1):65-66 MUSUMECI SA; FERRI R; BERGONZI P THE SPECIFICITY OF THE CHARACTERISTIC SLEEP EEG PATTERN IN THE FRAGILE-X SYNDROME	1	1
1385	0	2	730 1990 NUCLEIC ACIDS RESEARCH 18(3):692-692 HUPKES PE; VANBENNEKOM CA; VANOOST BA; OOSTRA BA RN1, A NEW POLYMORPHIC MARKER NEAR THE FRAGILE-X LOCUS - (HGM10 ASSIGNMENT DXS-369)	1	2
1386	2	3	736 1990 PRENATAL DIAGNOSIS 10(8):545-546 OOSTRA BA; SANDKUYL LA; HALLEY DJJ RISK CALCULATION OF MISSED PRENATAL-DIAGNOSIS OF FRAGILE-X SYNDROME	1	1
1387	0	0	761 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):231-231 SHAPIRO LR; WILMOT PL PRENATAL CYTOGENETIC DIAGNOSIS OF THE FRAGILE X-SYNDROME - DETERMINATION OF ACCURACY	1	1
1388	12	39	787 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):158-172 BROWN WT; JENKINS E; NERI G; LUBS H; SHAPIRO LR; et al. 4TH INTERNATIONAL WORKSHOP ON THE FRAGILE-X AND X-LINKED MENTAL-RETARDATION	1	7
1389	1	8	794 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):288-289 ZHAO Y; SHEN Y; LIU Y; ZHANG JC; YE LZ; et al. FRAGILE-X SYNDROME (MARTIN-BELL SYNDROME) IN CHINA	1	1
1390	7	20	798 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):311-318 CARPENTER NJ DNA LINKAGE ANALYSIS OF 26 FAMILIES WITH FRAGILE-X SYNDROME	1	1
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1391	14	31	800 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):322-327 GOONEWARDENA P; BROWN WT; GROSS AC; FERRANDO C; DOBKIN C; et al. LINKAGE ANALYSIS OF THE FRAGILE-X SYNDROME USING A NEW DNA MARKER U6.2 DEFINING LOCUS DXS304	1	1
1392	3	20	802 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):343-346 BROWN WT; GROSS AC; GOONEWARDENA P; FERRANDO C; DOBKIN C; et al. LINKAGE IN FRAGILE-X FAMILIES OF 3 DISTAL FLANKING MARKERS - ST14, DX13, AND F8	1	2
1393	1	7	816 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):416-417 JENKINS LS; GRUENERT DC; JENKINS EC; SCHONBERG SA TRANSFORMATION AND ESTABLISHMENT OF FRAGILE-X CELL-LINES FROM AMNIOCYTES	1	1
1394	6	20	819 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):429-433 KIMCHISARFATY C; GOITEIN R; KEREM B; WERNER M; MEIDAN B; et al. ENDOREDUPLICATION AND POLYPLOIDY IN FRAGILE-X CELLS INDUCED BY METHOTREXATE AND FLUORODEOXYURIDINE - IMPLICATIONS FOR DIAGNOSIS	1	3
1395	2	33	823 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):456-463 KRAWCZUN MS; JENKINS EC; DUNCAN CJ; STARKHOUCK SL; KUNAPORN S; et al. DISTRIBUTION OF AUTOSOMAL FRAGILE SITES IN SPECIMENS CULTURED FOR PRENATAL FRAGILE-X DIAGNOSIS	1	1
1396	1	8	824 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):464-466 JENKINS EC; BROOKS SE; STARKHOUCK SL; DUNCAN CJ; BROOKS SLS; et al. SV40-TRANSFORMED FRAGILE(X) AMNIOCYTES	1	1
1397	16	38	842 1991 BIOESSAYS 13(5):243-251 JORDAN BR FRAGILE X-LINKED MENTAL-RETARDATION AND THE DIFFICULTIES OF REVERSE GENETICS	1	1
1398	0	0	855 1991 CYTOGENETICS AND CELL GENETICS 56(3-4):221-221 SHAPIRO LR; EALLONARDO SJ; WILMOT PL INTERNAL CONTROL FOR SUCCESSFUL INDUCTION OF THE FRAGILE X-CHROMOSOME - OTHER FOLATE SENSITIVE FRAGILE SITE EXPRESSION ELIMINATED	1	1
1399	2	9	856 1991 CYTOGENETICS AND CELL GENETICS 58(3-4):2054-2055 BOUVET A; BASRUR PK A MARKER FRAGILE X-CHROMOSOME ASSOCIATED WITH BALDY CALF SYNDROME	1	1
1400	1	3	863 1991 CYTOGENETICS AND CELL GENETICS 58(3-4):2085-2085 RIGGINS GJ; SHERMAN SL; OOSTRA BA; FEITELL D; SUTCLIFFE JS; et al. A HIGHLY POLYMORPHIC DINUCLEOTIDE REPEAT, DXS 548, IS TIGHTLY LINKED TO THE FRAGILE-X SITE	1	2
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1401	9	23	866 1991 GENOMICS 10(4):1053-1060 DJABALI M; NGUYEN C; BIUNNO I; OOSTRA BA; MATTEI MG; et al. LASER MICRODISSECTION OF THE FRAGILE X REGION - IDENTIFICATION OF COSMID CLONES AND OF CONSERVED SEQUENCES IN THIS REGION	1	25
1402	6	9	876 1991 JOURNAL OF MEDICAL GENETICS 28(12):811-813 CONNOR JM CLONING OF THE GENE FOR THE FRAGILE-X SYNDROME - IMPLICATIONS FOR THE CLINICAL GENETICIST	1	1
1403	3	12	890 1991 NATURE 349(6312):742-743 CRAIG I HUMAN-GENETICS - METHYLATION AND THE FRAGILE-X	1	5
1404	0	16	901 1991 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 88(3):921-925 OBA T; ANDACHI Y; MUTO A; OSAWA S CGG - AN UNASSIGNED OR NONSENSE CODON IN MYCOPLASMA-CAPRICOLUM	1	49
1405	8	14	912 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 42(2):184-186 FINUCANE BM; JAEGER E; DUNN E; SCOTT CI STUDY OF COLOR-VISION IN FRAGILE-X SYNDROME	1	1
1406	10	14	929 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):136-141 JENKINS EC; GENOVESE MJ; DUNCAN CJ; GU H; STARKHOUCK SL; et al. FRA(X)(Q27.2), THE COMMON FRAGILE SITE, OBSERVED IN ONLY ONE OF 760 CASES STUDIED FOR THE FRAGILE-X SYNDROME	1	1
1407	11	21	930 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):142-148 FISCH GS; FRYNS JP FACTORS WHICH CONTRIBUTE TO CYTOGENETIC FREQUENCY OF EXPRESSION IN FAMILIES OF FRAGILE-X FEMALES	1	1
1408	12	19	931 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):155-160 JENKINS EC; DUNCAN CJ; GU H; GENOVESE M; KRAWCZUN MS DIALYZED FETAL BOVINE SERUM INCREASES CYTOGENETIC FRAGILE-X EXPRESSION	1	1
1409	4	6	935 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):170-173 SHAPIRO LR; WILMOT PL; FISCH GS PRENATAL CYTOGENETIC DIAGNOSIS OF THE FRAGILE-X SYNDROME IN AMNIOTIC-FLUID - CALCULATION OF ACCURACY	1	1
1410	11	12	937 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):181-186 MURPHY PD; WILMOT PL; SHAPIRO LR PRENATAL-DIAGNOSIS OF FRAGILE-X SYNDROME - RESULTS FROM PARALLEL MOLECULAR AND CYTOGENETIC STUDIES	1	1
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1411	7	22	951 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):312-319 CARPENTER NJ; SWARTZBOYD J; PRICHARD JK; LAM T LINKAGE AND RISK ASSESSMENT IN FRAGILE-X FAMILIES USING NEW DNA PROBES AT XQ27	1	1
1412	5	5	955 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):339-344 VIANNAMORGANTE AM; OTTO PA NOTES ON THE POPULATION-GENETICS OF FRAGILE X SYNDROME	1	1
1413	12	25	963 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 44(5):676-682 STROM CM; BRUSCA RM; PIZZI WJ DOUBLE-BLIND, PLACEBO-CONTROLLED CROSSOVER STUDY OF FOLINIC ACID (LEUCOVORIN(R)) FOR THE TREATMENT OF FRAGILE-X SYNDROME	1	3
1414	3	4	971 1992 ARCHIVES FRANCAISES DE PEDIATRIE 49(5):477-477 DROUIN V; VANNIER JP; MOIROT H; MITROFANOFF P; TRON P WILMS-TUMOR AND FRAGILE-X SYNDROME	1	1
1415	5	11	975 1992 BRITISH MEDICAL JOURNAL 305(6847):208-208 MOORE DWY NEW DEVELOPMENTS IN THE FRAGILE-X SYNDROME	1	1
1416	16	33	984 1992 EDUCATIONAL RESEARCH 34(3):221-228 GIBB C THE MOST COMMON-CAUSE OF LEARNING-DIFFICULTIES - A PROFILE OF FRAGILE-X SYNDROME AND ITS IMPLICATIONS FOR EDUCATION	1	1
1417	7	8	1002 1992 JOURNAL OF MEDICAL GENETICS 29(10):726-729 TARLETON J; WONG S; HEITZ D; SCHWARTZ C DIFFICULT DIAGNOSIS OF THE FRAGILE X-SYNDROME MADE POSSIBLE BY DIRECT DETECTION OF DNA MUTATIONS	1	1
1418	8	9	1004 1992 JOURNAL OF MEDICAL GENETICS 29(12):919-920 TARLETON J; WONG S; SCHWARTZ C DIRECT ANALYSIS OF THE FMR-1 GENE PROVIDES AN EXPLANATION FOR AN EXCEPTIONAL CASE OF A FRAGILE-X NEGATIVE, MENTALLY-RETARDED MALE IN A FRAGILE-X FAMILY	1	2
1419	19	25	1005 1992 JOURNAL OF PEDIATRICS 121(3):385-390 POTTER NT; LOZZIO CB; ANDERSON IJ; BOWLIN ES; MATTESON KJ USE OF A MOLECULAR GENETIC APPROACH TO DIAGNOSING THE FRAGILE-X GENOTYPE	1	1
1420	17	25	1011 1992 MEDICINA CLINICA 98(4):121-124 GINE R; ESPINAS ML; ANTICH J; CARBALLO M MOLECULAR-GENETICS OF THE FRAGILE-X SYNDROME - MOLECULAR DIAGNOSIS BY DNA PROBES	1	1
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1421	27	59	1025 1992 PSYCHIATRIC GENETICS 2(4):277-300 BOLTON P; PICKLES A; BUTLER L; SUMMERS D; WEBB T; et al. FRAGILE-X IN FAMILIES MULTIPLEX FOR AUTISM AND RELATED PHENOTYPES - PREVALENCE AND CRITERIA FOR CYTOGENETIC DIAGNOSIS	1	7
1422	19	26	1028 1992 ZEITSCHRIFT FUR KINDER-UND JUGENDPSYCHIATRIE UND PSYCHOTHERAPIE 20(2):113-120 VONGONTARD A; HILLIG U; HEROLD D CLINICAL AND CYTOGENETIC PROBLEMS IN THE DIAGNOSIS OF THE FRAGILE-X SYNDROME	1	1
1423	4	9	1029 1992 ZHURNAL NEVROPATOLOGII I PSIKHIATRII IMENI S S KORSAKOVA 92(4):28-31 LASTOCHKINA NA; KUPRIYANOVA TA; PUCHINSKAYA LM; MARINCHEVA GS; GORKOVA SA THE CLINICOELECTROPHYSIOLOGICAL CHARACTERIZATION OF WOMEN, HETEROZYGOUS CARRIERS OF FRAGILE X-CHROMOSOME	1	1
1424	23	29	1033 1993 AMERICAN JOURNAL OF DISEASES OF CHILDREN 147(11):1231-1235 RAMOS FJ; EUNPU DL; FINUCANE B; PFENDNER EG DIRECT DNA TESTING FOR FRAGILE-X SYNDROME	1	2
1425	0	0	1040 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):78-78 ROUSSEAU F; HEITZ D; TARLETON J; MACPHERSON J; PETTERSON U; et al. A COLLABORATIVE MULTICENTER STUDY OF DIRECT DIAGNOSIS OF THE FRAGILE-X SYNDROME WITH PROBE STB12.3 - THE 1ST 2253 CASES	1	1
1426	0	0	1043 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):144-144 HAGERMAN R; HULL C; CARPENTER I; STALEY L; OCONNOR R; et al. HIGH-FUNCTIONING FRAGILE X MALES	1	1
1427	0	0	1047 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):448-448 HOLDEN JJA; CHALIFOUX M; WING M; WHITE BN; GLOVER T; et al. THE FRAGILE-X SYNDROME AND PREMATURE MENOPAUSE	1	1
1428	0	0	1050 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):678-678 EBERHART DE; WARREN ST ABNORMAL CHROMATIN STRUCTURE ASSOCIATED WITH THE FULL FRAGILE-X MUTATION	1	2
1429	0	0	1051 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):717-717 PERGOLIZZI RG; ERSTER SH; MILLAN CA; GUZOWSKI DE; SELLATI LM STABILITY OF THE CGG REPEAT REGION OF FMR-1	1	1
1430	0	0	1063 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):1241-1241 TORRES W; SAHOTA A; BOYADJIEV S; VANCE GH; WEAVER DD FRAGILE-X FULL MUTATION IN 2 CLINICALLY UNAFFECTED BROTHERS	1	2
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1431	0	0	1082 1993 ANNALES DE PEDIATRIE 40(9):565-572 BLANC DS; DANGELO J; ETANGS NLD AUTISM AND THE FRAGILE X-SYNDROME	1	1
1432	0	0	1120 1993 IRISH MEDICAL JOURNAL 86(3):92-& KEENAN E; KEANE V; RAMSEY L FRAGILE-X SYNDROME - A REVIEW	1	1
1433	10	11	1132 1993 JOURNAL OF MEDICAL GENETICS 30(3):193-197 KNOBLOCH O; PELZ F; WICK U; NELSON DL; ZOLL B DIRECT VERSUS INDIRECT MOLECULAR DIAGNOSIS OF FRAGILE-X MENTAL-RETARDATION IN 40 GERMAN FAMILIES AT RISK	1	1
1434	7	9	1137 1993 JOURNAL OF MEDICAL GENETICS 30(9):785-787 SUZUMORI K; YAMAUCHI M; SEKI N; KONDO I; HORI T PRENATAL-DIAGNOSIS OF A HYPERMETHYLATED FULL FRAGILE-X MUTATION IN CHORIONIC VILLI OF A MALE FETUS	1	5
1435	6	7	1143 1993 LANCET 342(8878):1004-1005 YOUNG ID DIAGNOSING FRAGILE-X SYNDROME	1	1
1436	17	34	1146 1993 MEDICAL JOURNAL OF AUSTRALIA 158(7):482-485 SUTHERLAND GR; MULLEY JC; RICHARDS RI FRAGILE-X SYNDROME - THE MOST COMMON CAUSE OF FAMILIAL INTELLECTUAL HANDICAP	1	5
1437	3	6	1185 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):374-377 STEYAERT J; BORGHGRAEF M; FRYNS JP APPARENTLY ENHANCED VISUAL INFORMATION-PROCESSING IN FEMALE FRAGILE-X CARRIERS - PRELIMINARY FINDINGS	1	1
1438	4	7	1190 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):403-404 SCHAAP C; FRYNS JP SEVERE PROGRESSIVE NEUROLOGICAL DISORDER ASSOCIATED WITH HYDROCEPHALUS IN A MAN WITH FRAGILE-X-SYNDROME	1	2
1439	5	8	1193 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):436-442 JENKINS EC; MORYS I; HENDERSON J; GENOVESE M; CARTER M; et al. FRAGILE-X INDUCTION SYSTEMS IN CVS CULTURES - EFFECT ON CYTOGENETIC, PCR, AND GENOMIC SOUTHERN BLOT DNA ANALYSES OF THE FMR-1 GENE	1	1
1440	7	8	1197 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):452-453 JENKINS EC; GENOVESE M; DUNCAN CJ; GU H; STARKHOUCK S; et al. OCCURRENCE OF ANEUPLOIDY FOR THE X-CHROMOSOME IN OVER 1,300 UNRELATED SPECIMENS SCREENED FOR THE FRAGILE X-CHROMOSOME	1	1
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1441	14	17	1215 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 53(4):370-373 PUISSANT H; MALINGE MC; LARGETPIET A; MARTIN D; CHAUVEAU P; et al. MOLECULAR ANALYSIS OF 53 FRAGILE-X FAMILIES WITH THE PROBE-STB12.3	1	2
1442	9	28	1218 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 54(2):141-143 CRADDOCK N; DANIELS J; MCGUFFIN P; OWEN M VARIATION AT THE FRAGILE X-LOCUS DOES NOT INFLUENCE SUSCEPTIBILITY TO BIPOLAR DISORDER	1	6
1443	14	28	1224 1994 BRITISH JOURNAL OF CLINICAL PRACTICE 48(1):42-44 PATEL BD THE FRAGILE-X SYNDROME	1	1
1444	1	16	1226 1994 CANCER RESEARCH 54(19):5212-5216 LEE ST; MCGLENNEN RC; LITZ CE CLONAL DETERMINATION BY THE FRAGILE-X (FMR1) AND PHOSPHOGLYCERATE KINASE (PGK) GENES IN HEMATOLOGICAL MALIGNANCIES	1	12
1445	0	19	1234 1994 GENES CHROMOSOMES & CANCER 9(2):141-144 RIGGINS GJ; SHERMAN SL; PHILLIPS CN; STOCK W; WESTBROOK CA; et al. CGG-REPEAT POLYMORPHISM OF THE BCR GENE RULES OUT PREDISPOSING ALLELES LEADING TO THE PHILADELPHIA-CHROMOSOME	1	8
1446	1	1	1249 1994 JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION 271(1):28-28 BROWN WT; HOUCK GE; JEZIOROWSKA A; LEVINSON FN; DING X; et al. RAPID FRAGILE-X CARRIER SCREENING AND PRENATAL-DIAGNOSIS USING A NONRADIOACTIVE PCR TEST (VOL 270, PG 1569, 1993)	1	1
1447	9	20	1256 1994 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 38:1-8 DEVRIES LBA; HALLEY DJJ; OOSTRA BA; NIERMEIJER MF THE FRAGILE-X SYNDROME - A GROWING GENE CAUSING FAMILIAL INTELLECTUAL DISABILITY	1	2
1448	1	2	1263 1994 JOURNAL OF MEDICAL GENETICS 31(10):820-820 DEVRIES BBA; NIERMEIJER MF THE PRADER-WILLI-LIKE PHENOTYPE IN FRAGILE-X PATIENTS - A DESIGNATION FACILITATING CLINICAL (AND MOLECULAR) DIFFERENTIAL-DIAGNOSIS	1	6
1449	6	12	1264 1994 JOURNAL OF MEDICAL GENETICS 31(12):950-952 CURTIS G; DENNIS N; MACPHERSON J THE IMPACT OF GENETIC-COUNSELING ON FEMALES IN FRAGILE-X FAMILIES	1	1
1450	0	0	1279 1994 PEDIATRIC RESEARCH 35(4):A23-A23 LACHIEWICZ AM; DAWSON DV AUTISTIC BEHAVIORS OF YOUNG GIRLS WITH FRAGILE X-SYNDROME	1	1
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1451	10	22	1362 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):223-229 King RA; Hagerman R; Houghton M Ocular findings in fragile X syndrome	1	1
1452	27	36	1363 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):230-241 Brun C; Obiols JE; Cheema A; OConnor R; Riddle J; et al. Longitudinal IQ changes in fragile X females	1	1
1453	26	41	1368 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):293-301 Jenkins EC; Houck GE; Ding XH; Li SY; StarkHouck SL; et al. An update on fragile X prenatal diagnosis: End of the cytogenetic testing era	1	1
1454	2	9	1390 1995 GENETIC COUNSELING 6(3):207-210 ALEMBIK Y; DOTT B; STOLL C RETT-LIKE SYNDROME IN FRAGILE-X SYNDROME	1	6
1455	12	26	1392 1995 GENETIC EPIDEMIOLOGY 12(3):279-290 HUGGINS RM; LOESCH DZ USE OF ROBUST STATISTICAL-METHODS TO DETERMINE THE EFFECT OF FRAGILE-X ON MEANS AND VARIANCE-COMPONENTS OF A QUANTITATIVE TRAIT	1	2
1456	8	11	1399 1995 ISRAEL JOURNAL OF MEDICAL SCIENCES 31(5):323-325 DAR H; SCHAAP T; BAITOR H; BOROCHOWITZ Z; GELMANKOHAN Z; et al. ETHNIC DISTRIBUTION OF THE FRAGILE-X SYNDROME IN ISRAEL - EVIDENCE OF FOUNDER CHROMOSOMES()	1	1
1457	4	21	1456 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):27-30 Carrel L; Willard HF An assay for X inactivation based on differential methylation at the fragile X locus, FMR1	1	32
1458	9	10	1459 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):187-190 Grasso M; Perroni L; Colella S; Piombo G; Argusti A; et al. Prenatal diagnosis of 30 fetuses at risk for fragile X syndrome	1	2
1459	10	14	1488 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):362-364 Fisch GS; Carpenter N; HowardPeebles PN; Maddalena A; Simensen R; et al. Lack of association between mutation size and cognitive/behavior deficits in fragile X males: A brief report	1	3
1460	3	18	1494 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):395-398 Piussan C; Mathieu M; Berquin P; Fryns JP Fragile X mutation and FG syndrome-like phenotype	1	4
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1461	14	19	1495 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):404-407 Kambouris M; Snow K; Thibodeau S; Bluhm D; Green M; et al. Segregation of the fragile X mutation from a male with a full mutation: Unusual somatic instability in the FMR-1 locus	1	3
1462	10	25	1505 1996 ANNALS OF CLINICAL AND LABORATORY SCIENCE 26(4):323-328 Mark HFL; Bier JAB; Scola P The frequency of chromosomal abnormalities in patients referred for fragile X analysis	1	4
1463	4	13	1509 1996 ARCHIVES OF MEDICAL RESEARCH 27(4):587-588 Rivera H Fragile X studies and authorship	1	5
1464	64	95	1517 1996 CHILD AND ADOLESCENT PSYCHIATRIC CLINICS OF NORTH AMERICA 5(4):895-& Hagerman RJ Fragile X syndrome	1	9
1465	11	21	1522 1996 CLINICAL OBSTETRICS AND GYNECOLOGY 39(4):772-782 Finucane B Should all pregnant women be offered carrier testing for fragile X syndrome?	1	1
1466	1	4	1557 1996 JOURNAL OF SLEEP RESEARCH 5(4):272-272 Musumeci SA; Ferri R; Elia M; DelGracco S; Scuderi C; et al. Normal respiratory pattern during sleep in young fragile X-syndrome patients	1	1
1467	3	45	1560 1996 MEDICAL ANTHROPOLOGY QUARTERLY 10(4):537-550 Nelkin D The social dynamics of genetic testing: The case of Fragile-X	1	6
1468	4	138	1561 1996 MEDICAL HYPOTHESES 47(4):289-298 Fischer KM Genes for Prader Willi Syndrome Angelman syndrome and fragile X syndrome are homologous, with genetic imprinting and unstable trinucleotide repeats causing mental retardation, autism and aggression	1	4
1469	16	28	1572 1996 PSYCHIATRIC GENETICS 6(2):81-86 Ashworth A; Abusaad I; Walsh C; Nanko S; Murray RM; et al. Linkage analysis of the fragile X gene FMR-1 and schizophrenia: No evidence for linkage but report of a family with schizophrenia and an unstable triplet repeat	1	3
1470	8	27	1573 1996 PSYCHIATRY RESEARCH 64(2):97-104 Thompson NM; Rogeness GA; McClure E; Clayton R; Johnson C Influence of depression on cognitive functioning in Fragile X females	1	6
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1471	0	0	1594 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A30-A30 Gunter C; Paradee W; Newman J; Sherman SL; Warren ST A novel biallelic polymorphism in the FMR1 gene shows strong linkage disequilibrium With CGG repeats and flanking microsatellite markers.	1	1
1472	0	0	1610 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A306-A306 Chiurazzi P; Pomponi MG; Willemsen R; Oostra BA; Neri G In vitro reactivation of the fragile X syndrome gene.	1	1
1473	0	0	1612 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A316-A316 Nolin SL; Houck GE; Blumstein H; Ye LL; Dobkin CS; et al. Single cell analysis shows different FMR1 CGG repeat stability in sperm and lymphocytes of premutation males.	1	2
1474	0	0	1613 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A321-A321 Tassone F; Hagerman RJ; Ikle D; Dyer PN; Lampe M; et al. FMRP expression as a potential prognostic indicator in fragile X syndrome.	1	1
1475	4	11	1642 1997 BRITISH MEDICAL JOURNAL 315(7117):1174-1175 Barnicoat A Screening for fragile X syndrome: a model for genetic disorders?	1	4
1476	10	16	1651 1997 DIAGNOSTIC MOLECULAR PATHOLOGY 6(3):161-166 Marini T; Pflueger S; Jackson A; Naber S; Karpells S; et al. A five-year experience with fragile X testing - Setting laboratory standards of practice and a cost-effective protocol	1	2
1477	13	28	1653 1997 EUROPEAN JOURNAL OF HUMAN GENETICS 5(2):89-93 FulchignoniLataud MC; Olchwang S; Serre JL The fragile X CGG repeat shows a marked level of instability in hereditary non-polyposis colorectal cancer patients	1	6
1478	6	15	1656 1997 GENETIC COUNSELING 8(1):1-6 Patsalis PC; Sismani C; Hadjimarcou MI; Rose N; Stylianidou G; et al. Cytogenetic and fragile X molecular testing of individuals with mental retardation of unknown etiology	1	3
1479	1	2	1683 1997 JOURNAL OF MEDICAL GENETICS 34(4):350-350 Loesch DZ FMR1 fully expanded mutation with minimal methylation in a high functioning fragile X male	1	1
1480	11	15	1687 1997 JOURNAL OF MEDICAL GENETICS 34(11):924-926 Losekoot M; Hoogendoorn E; Olmer R; Jansen CCAM; Oosterwijk JC; et al. Prenatal diagnosis of the fragile X syndrome: loss of mutation owing to a double recombinant or gene conversion event at the FMR1 locus	1	7
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1481	1	1	1697 1997 NATURE STRUCTURAL BIOLOGY 4(10):840-840 Musco G; Kharrat A; Stier G; Fraternali F; Gibson TJ; et al. The solution structure of the first KH domain of FMR1, the protein responsible for the fragile X syndrome (vol 4, pg 712, 1997)	1	2
1482	23	44	1706 1997 PSYCHIATRIC GENETICS 7(3):115-119 ODwyer J; Holmes J; Mueller R; Taylor G The prevalence of Fragile-X syndrome in an institution for people with learning disability	1	3
1483	31	49	1708 1997 REVISTA DE NEUROLOGIA 25(143):1068-1071 EstevezGonzalez A; Roig C; Piles S; Pineda M; GarciaSanchez C Fragile-X syndrome and mental retardation	1	1
1484	20	30	1720 1998 ANNALS OF HUMAN GENETICS 62:337-347 Huggins RM; Loesch DZ; Sherman SL A branching non-linear autoregressive model for the transmission of the fragile X dynamic repeat mutation	1	2
1485	31	107	1731 1998 CURRENT OPINION IN GENETICS & DEVELOPMENT 8(2):245-253 Tapscott SJ; Klesert TR; Widrow RJ; Stoger R; Laird CD Fragile-X syndrome and myotonic dystrophy: parallels and paradoxes	1	10
1486	12	14	1732 1998 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 40(1):62-64 Gringras P; Barnicoat A Retesting for fragile X syndrome in cytogenetically normal males	1	3
1487	4	7	1747 1998 HUMAN GENETICS 102(1):54-56 Storm K; Handig I; Reyniers E; Oostra BA; Kooy RF; et al. Incomplete EcoRI digestion may lead to false diagnosis of fragile X syndrome	1	1
1488	17	40	1784 1998 JOURNAL OF NEUROSCIENCE RESEARCH 51(1):41-48 Berry-Kravis E; Ciurlionis R Overexpression of fragile X gene (FMR-1) transcripts increases cAMP production in neural cells	1	1
1489	30	41	1795 1998 REVISTA MEDICA DE CHILE 126(8):911-918 Jara L; Lopez M; Mellado C; Aspillaga M; Avendano I; et al. Clinical and metabolic screening for fragile X syndrome in 300 patients with unspecific mental retardation	1	1
1490	10	25	1796 1998 REVISTA MEDICA DE CHILE 126(12):1447-1454 Aspillaga M; Jara L; Avendano I; Lopez M Fragile X syndrome. Clinical analysis of 300 Chilean patients with unspecific mental retardation	1	1
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1491	38	61	1824 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):221-236 Holden JJA; Percy M; Allingham-Hawkins D; Brown WT; Chiurazzi P; et al. Eighth International Workshop on the Fragile X Syndrome and X-linked Mental Retardation, August 16-22, 1997	1	4
1492	13	22	1852 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):217-220 Patsalis PC; Sismani C; Stylianou S; Ioannou P; Joseph G; et al. Genetic variation and intergenerational FMR1 CGG-repeat stability in 100 unrelated three-generation families from the normal population	1	2
1493	18	22	1855 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):229-232 Petek E; Kroisel PM; Schuster M; Zierler H; Wagner K Mosaicism in a fragile X male including a de novo deletion in the FMR1 gene	1	1
1494	5	13	1864 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 85(3):197-201 Freedenberg DL; Gane LW; Richards CS; Lampe M; Hills J; et al. Fragile X syndrome and an isodicentric X chromosome in a woman with multiple anomalies, developmental delay, and normal pubertal development	1	1
1495	10	14	1865 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 85(3):311-316 Grasso M; Faravelli F; Lo Nigro C; Chiurazzi P; Sperandeo MP; et al. Mosaicism for the full mutation and a microdeletion involving the CGG repeat and flanking sequences in the FMR1 gene in eight fragile X patients	1	1
1496	7	12	1866 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 86(2):162-164 Sun YJ; Baumer A Nonrandom X inactivation and selection of fragile X full mutation in fetal fibroblasts	1	3
1497	17	24	1870 1999 AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY 181(4):789-792 Wenstrom KD; Descartes M; Franklin J; Cliver SP A five-year experience with fragile X screening of high-risk gravid women	1	1
1498	0	0	1873 1999 ARCHIVES OF CLINICAL NEUROPSYCHOLOGY 14(8):767-768 Lanham DC; Mazzocco MM; Denckla MB Depression and anxiety in girls with Fragile X or Turner Syndrome.	1	1
1499	15	19	1878 1999 CLINICAL CHEMISTRY AND LABORATORY MEDICINE 37(4):397-401 Houdayer C; Lemonnier A; Gerard M; Chauve C; Tredano M; et al. Improved fluorescent PCR-based assay for sizing CGG repeats at the FRAXA locus	1	6
1500	6	14	1896 1999 GENETICS AND MOLECULAR BIOLOGY 22(4):471-474 Vianna-Morgante AM; Costa SS; Pavanello RDM; Otto PA; Mingroni-Netto RC Premature ovarian failure (POF) in Brazilian fragile X carriers	1	4

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