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Nodes: 2369
Authors: 4634,
Journals: 373,
Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by GCS.
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| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 1201 | 1 | 5 | 802 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):378-379 DOBKIN CS; DRISCOLL MC; FERRANDO C POLYMERASE CHAIN-REACTION DETECTION OF THE DDE-I POLYMORPHISM IN THE FACTOR-IX GENE FOR FRAGILE-X LINKAGE ANALYSIS | 0 | 3 |
| 1202 | 0 | 4 | 808 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):408-410 SHAPIRO LR; WILMOT PL; SHAPIRO DA; PETTERSEN IM; CASAMASSIMA AC CYTOGENETIC DIAGNOSIS OF THE FRAGILE-X SYNDROME - EFFICIENCY, UTILIZATION, AND TRENDS | 3 | 3 |
| 1203 | 6 | 20 | 812 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):429-433 KIMCHISARFATY C; GOITEIN R; KEREM B; WERNER M; MEIDAN B; SCHAAP T ENDOREDUPLICATION AND POLYPLOIDY IN FRAGILE-X CELLS INDUCED BY METHOTREXATE AND FLUORODEOXYURIDINE - IMPLICATIONS FOR DIAGNOSIS | 1 | 3 |
| 1204 | 2 | 9 | 911 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):61-64 REISS AL; CIANCHETTI C; COHEN IL; DEVRIES B; HAGERMAN R; HINTON V; FROSTER U; LACHIEWICZ A; MAZZOCCO M; SOBESKY W; SUDHALTER V BRIEF SCREENING QUESTIONNAIRE FOR DETERMINING AFFECTED STATE IN FRAGILE-X SYNDROME - A CONSENSUS RECOMMENDATION | 2 | 3 |
| 1205 | 6 | 10 | 919 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):120-123 PARTINGTON MW; ROBINSON H; LAING S; TURNER G MORTALITY IN THE FRAGILE-X SYNDROME - PRELIMINARY DATA | 2 | 3 |
| 1206 | 6 | 12 | 925 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):162-166 HOWARDPEEBLES PN; MADDALENA A RECENT EXPERIENCE IN PRENATAL-DIAGNOSIS OF FRAGILE-X | 3 | 3 |
| 1207 | 12 | 25 | 928 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):174-180 VONKOSKULL H; NORDSTROM AM; SALONEN R; PELTONEN L PRENATAL-DIAGNOSIS AND CARRIER DETECTION IN FRAGILE-X | 3 | 3 |
| 1208 | 12 | 25 | 954 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 |
| 1209 | 38 | 77 | 969 1992 CLINICAL SCIENCE 83(3):255-264 HIRST MC; KNIGHT SJL; BELL MV; SUPER M; DAVIES KE THE FRAGILE-X SYNDROME | 2 | 3 |
| 1210 | 23 | 48 | 973 1992 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 34(9):826-832 GOLDSON E; HAGERMAN RJ THE FRAGILE-X SYNDROME | 3 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1211 | 37 | 55 | 980 1992 HUMAN GENETICS 88(3):335-343 FOLLETTE PJ; LAIRD CD ESTIMATING THE STABILITY OF THE PROPOSED IMPRINTED STATE OF THE FRAGILE-X MUTATION WHEN TRANSMITTED BY FEMALES | 2 | 3 |
| 1212 | 1 | 11 | 1062 1993 AMERICAN JOURNAL OF MEDICAL GENETICS 46(6):685-686 MIGEON BR ROLE OF DNA METHYLATION IN X-INACTIVATION AND THE FRAGILE X-SYNDROME | 2 | 3 |
| 1213 | 4 | 14 | 1079 1993 CLINICAL GENETICS 44(2):82-88 LOESCH DZ; SAMPSON ML EFFECT OF THE FRAGILE-X ANOMALY ON BODY PROPORTIONS ESTIMATED BY PEDIGREE ANALYSIS | 3 | 3 |
| 1214 | 9 | 24 | 1130 1993 MENTAL RETARDATION 31(4):221-227 WILSON PG; MAZZOCCO MMM AWARENESS AND KNOWLEDGE OF FRAGILE-X SYNDROME AMONG SPECIAL EDUCATORS | 2 | 3 |
| 1215 | 18 | 21 | 1131 1993 MENTAL RETARDATION 31(5):279-283 SMITH SE COGNITIVE DEFICITS ASSOCIATED WITH FRAGILE-X SYNDROME | 2 | 3 |
| 1216 | 8 | 9 | 1157 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):315-316 BUTLER MG; PRATESI R; VNENCAKJONES CL MOLECULAR-GENETIC SCREENING IN CYTOGENETICALLY NORMAL MENTALLY-RETARDED MALES WITH MANIFESTATIONS OF FRAGILE-X-SYNDROME | 2 | 3 |
| 1217 | 1 | 4 | 1176 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):451-451 SCHMIDT M; ROBERTSON A; CRAWFORD M X INACTIVATION PATTERN IN INTERSTITIAL DELETIONS OF THE FRAGILE-X REGION | 0 | 3 |
| 1218 | 1 | 3 | 1238 1994 JOURNAL OF MEDICAL GENETICS 31(3):260-261 GILLESSENKAESBACH G; HORSTHEMKE B CLINICAL AND MOLECULAR STUDIES IN FRAGILE-X PATIENTS WITH A PRADER-WILLI-LIKE PHENOTYPE | 0 | 3 |
| 1219 | 0 | 0 | 1266 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):153-153 BLACK SH; LEVINSON G; HARTON GL; PALMER FT; SISSON ME; SCHOENER C; NANCE C; FUGGER EF; FIELDS RA PREIMPLANTATION GENETIC TESTING (PGT) FOR FRAGILE-X (FRAX) | 2 | 3 |
| 1220 | 2 | 5 | 1295 1995 AMERICAN JOURNAL OF MEDICAL GENETICS 57(3):508-509 LAXOVA R FRAGILE-X SCREENING - WHAT IS THE REAL ISSUE | 2 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1221 | 0 | 1 | 1318 1995 BRITISH MEDICAL JOURNAL 310(6973):148-148 CRAFT N STUDY SUPPORTS SCREENING FOR THE FRAGILE-X-SYNDROME | 2 | 3 |
| 1222 | 32 | 75 | 1324 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):187-198 Abrams MT; Reiss AL Quantitative brain imaging studies of fragile X syndrome | 2 | 3 |
| 1223 | 3 | 16 | 1326 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):218-222 Musumeci SA; Ferri R; Elia M; DalGracco S; Scuderi C; Stefanini MC; Castano A; Azan G Sleep neurophysiology in fragile X patients | 2 | 3 |
| 1224 | 1 | 4 | 1353 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 |
| 1225 | 10 | 14 | 1437 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):362-364 Fisch GS; Carpenter N; HowardPeebles PN; Maddalena A; Simensen R; Tarleton J; JulienInalsingh C; Chalifoux M; Holden JJA Lack of association between mutation size and cognitive/behavior deficits in fragile X males: A brief report | 1 | 3 |
| 1226 | 2 | 2 | 1440 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):376-376 Burgess B; Partington M; Turner G; Robinson H Normal age of menarche in fragile X syndrome | 3 | 3 |
| 1227 | 4 | 6 | 1441 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):377-377 HowardPeebles PN Successful pregnancy in a fragile X carrier by donor egg | 2 | 3 |
| 1228 | 14 | 19 | 1444 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):404-407 Kambouris M; Snow K; Thibodeau S; Bluhm D; Green M; Feldman GL Segregation of the fragile X mutation from a male with a full mutation: Unusual somatic instability in the FMR-1 locus | 1 | 3 |
| 1229 | 16 | 28 | 1511 1996 PSYCHIATRIC GENETICS 6(2):81-86 Ashworth A; Abusaad I; Walsh C; Nanko S; Murray RM; Asherson P; McGuffin P; Gill M; Owen MJ; Collier DA 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 |
| 1230 | 6 | 15 | 1586 1997 GENETIC COUNSELING 8(1):1-6 Patsalis PC; Sismani C; Hadjimarcou MI; Rose N; Stylianidou G; Koukoulli R; Anastasiadou V; Deltas CC; Middleton L Cytogenetic and fragile X molecular testing of individuals with mental retardation of unknown etiology | 1 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1231 | 11 | 19 | 1587 1997 GENETIC TESTING 1(3):151-155 Das S; Kubota T; Song M; Daniel R; Berry-Kravis EM; Prior TW; Popovich B; Rosser L; Arinami T; Ledbetter DH Methylation analysis of the fragile X syndrome by PCR | 2 | 3 |
| 1232 | 10 | 16 | 1592 1997 HUMAN GENETICS 101(2):186-189 Pesso R; Barkai G; Ravia Y; Gak E; Frydman M; Goldman B; Friedman E No founder effect detected in Jewish Ashkenazi patients with fragile-X syndrome | 2 | 3 |
| 1233 | 7 | 12 | 1646 1998 CLINICAL GENETICS 54(4):366-367 Vatta S; Cigui I; Demori E; Morgutti M; Pecile V; Benussi DG; Serra C; Amoroso A Fragile X syndrome, mental retardation and macroorchidism | 3 | 3 |
| 1234 | 12 | 14 | 1648 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 |
| 1235 | 14 | 26 | 1669 1998 INDIAN JOURNAL OF MEDICAL RESEARCH 108:12-16 Jain U; Verma IC; Kapoor AK Prevalence of fragile X(A) syndrome in mentally retarded children at a genetics referral centre in Delhi, India | 2 | 3 |
| 1236 | 20 | 36 | 1690 1998 JOURNAL OF PEDIATRICS 133(3):363-365 Meyer GA; Blum NJ; Hitchcock W; Fortina P Absence of the fragile X CGG trinucleotide repeat expansion in girls diagnosed with a pervasive developmental disorder | 0 | 3 |
| 1237 | 3 | 9 | 1739 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):331-333 Wen GY; Jenkins EC; Goldberg EM; Genovese M; Brown WT; Wisniewski HM Ultrastructure of the fragile X chromosome: New observations on the fragile site | 0 | 3 |
| 1238 | 6 | 11 | 1740 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):338-341 Dobkin C; Ding XH; Li SY; Houck G; Nolin SL; Glicksman A; Zhong N; Jenkins EC; Brown WT Accelerated prenatal diagnosis of fragile X syndrome by polymerase chain reaction restriction fragment detection | 2 | 3 |
| 1239 | 4 | 5 | 1746 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):202-203 Tuncbilek E; Alikasifoglu M; Boduroglu K; Aktas D; Anar B Frequency of fragile X syndrome among Turkish patients with mental retardation of unknown etiology | 3 | 3 |
| 1240 | 20 | 26 | 1747 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 | 0 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1241 | 10 | 14 | 1748 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 | 1 | 3 |
| 1242 | 7 | 12 | 1762 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 |
| 1243 | 8 | 12 | 1774 1999 CLINICAL GENETICS 56(1):98-99 Millan JM; Martinez F; Cadroy A; Gandia J; Casquero M; Beneyto M; Badin L; Prieto F Screening for FMR1 mutations among the mentally retarded: prevalence of the fragile X syndrome in Spain | 2 | 3 |
| 1244 | 5 | 6 | 1810 1999 JOURNAL OF MEDICAL GENETICS 36(7):565-566 Moore SJ; Strain L; Cole GF; Miedzybrodzka Z; Kelly KF; Dean JCS Fragile X syndrome with FMR1 and FMR2 deletion | 1 | 3 |
| 1245 | 16 | 33 | 1857 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 | 3 |
| 1246 | 20 | 37 | 1867 2000 ANNALES DE GENETIQUE 43(1):29-34 Gonzalez-del Angel A; Vidal S; Saldana Y; del Castillo V; Alcantara MA; Macias M; Luna JP; Orozco L Molecular diagnosis of the fragile X and FRAXE syndromes in patients with mental retardation of unknown cause in Mexico | 2 | 3 |
| 1247 | 5 | 8 | 1870 2000 AUSTRALIAN AND NEW ZEALAND JOURNAL OF MEDICINE 30(1):86-88 Driscoll G; Clark J; Elakis G; Turner G Early menopause in a family carrying a fragile X premutation | 1 | 3 |
| 1248 | 8 | 18 | 1956 2000 NEUROSCIENCE RESEARCH COMMUNICATIONS 26(3):265-277 Bakker CE; Kooy RF; D'Hooge R; Tamanini F; Willemsen R; Nieuwenhuizen I; De Vries BBA; Reyniers E; Hoogeveen AT; Willems PJ; De Deyn PP; Oostra BA Introduction of a FMR1 transgene in the fragile X knockout mouse. | 3 | 3 |
| 1249 | 6 | 26 | 1982 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 |
| 1250 | 7 | 18 | 1984 2001 AMERICAN JOURNAL OF MEDICAL GENETICS 100(2):110-115 Stoll C Problems in the diagnosis of fragile X syndrome in young children are still present | 3 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1251 | 26 | 32 | 1996 2001 ANNALS OF CLINICAL BIOCHEMISTRY 38:264-271 Saha S; Karmakar P; Chatterjee C; Banerjee D; Das S; Dasgupta UB Fragile X syndrome in Calcutta, India | 1 | 3 |
| 1252 | 5 | 48 | 2021 2001 GENOME RESEARCH 11(8):1382-1391 Mathews DJ; Kashuk C; Brightwell G; Eichler EE; Chakravarti A Sequence variation within the fragile x locus | 0 | 3 |
| 1253 | 22 | 64 | 2024 2001 HUMAN MOLECULAR GENETICS 10(24):2803-2811 Huot ME; Mazroui R; Leclerc P; Khandjian EW Developmental expression of the fragile X-related 1 proteins in mouse testis: association with microtubule elements | 3 | 3 |
| 1254 | 15 | 47 | 2041 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 |
| 1255 | 8 | 20 | 2049 2001 NEUROREPORT 12(11):2573-2576 Rojas DC; Benkers TL; Rogers SJ; Teale PD; Reite ML; Hagerman RJ Auditory evoked magnetic fields in adults with fragile X syndrome | 2 | 3 |
| 1256 | 68 | 102 | 2076 2001 SEMINARS IN REPRODUCTIVE MEDICINE 19(2):159-165 Kenneson A; Warren ST The female and the fragile X reviewed | 1 | 3 |
| 1257 | 25 | 43 | 2098 2002 AMERICAN JOURNAL OF MEDICAL GENETICS 110(3):226-233 Crawford DC; Meadows KL; Newman JL; Taft LF; Scott E; Leslie M; Shubek L; Holmgreen P; Yeargin-Allsopp M; Boyle C; Sherman SL Prevalence of the fragile x syndrome in African-Americans | 2 | 3 |
| 1258 | 6 | 18 | 2113 2002 CLINICAL GENETICS 61(1):13-20 O'Connell CD; Atha DH; Jakupciak JP; Richie KI Standardization of PCR amplification for fragile X trinucleotide repeat measurements | 0 | 3 |
| 1259 | 11 | 20 | 2115 2002 CURRENT BIOLOGY 12(24):R852-R854 Carthew RW RNA interference: The fragile X syndrome connection | 0 | 3 |
| 1260 | 6 | 29 | 2153 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1261 | 62 | 98 | 2157 2002 JOURNAL OF NEUROSCIENCE RESEARCH 70(5):623-630 Todd PK; Malter JS Fragile X mental retardation protein in plasticity and disease | 1 | 3 |
| 1262 | 39 | 64 | 2164 2002 MICROSCOPY RESEARCH AND TECHNIQUE 57(3):148-155 Hoogeveen AT; Willemsen R; Oostra BA Fragile X syndrome, the fragile X related proteins, and animal models | 1 | 3 |
| 1263 | 25 | 35 | 2168 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 |
| 1264 | 17 | 39 | 2178 2002 NEUROBIOLOGY OF DISEASE 11(1):53-63 Schenck A; Van de Bor V; Bardoni B; Giangrande A Novel features of dFMR1, the Drosophila orthologue of the fragile X mental retardation protein | 3 | 3 |
| 1265 | 23 | 59 | 2179 2002 NEUROBIOLOGY OF DISEASE 11(1):221-229 Castren M; Lampinen KE; Miettinen R; Koponen E; Sipola I; Bakker CE; Oostra BA; Castren E BDNF regulates the expression of fragile X mental retardation protein mRNA in the hippocampus | 2 | 3 |
| 1266 | 26 | 80 | 2189 2002 OBSTETRICS AND GYNECOLOGY CLINICS OF NORTH AMERICA 29(2):367-+ Wenstrom KD Fragile X and other trinucleotide repeat diseases | 1 | 3 |
| 1267 | 18 | 22 | 2192 2002 PRENATAL DIAGNOSIS 22(6):459-462 Rife M; Mallolas J; Badenas C; Tazon B; Miguelez MR; Pampols T; Sanchez A; Mila M Pilot study for the neonatal screening of fragile X syndrome | 3 | 3 |
| 1268 | 5 | 14 | 2224 2003 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 117A(1):6-9 Hundscheid RDL; Smits APT; Thomas CMG; Kiemeney LALM; Braat DDM Female carriers of fragile X premutations have no increased risk for additional diseases other than premature ovarian failure | 0 | 3 |
| 1269 | 20 | 41 | 2227 2003 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 118A(2):127-134 Loesch DZ; Huggins RM; Bui QM; Taylor AK; Hagerman RJ Relationship of deficits of FMR1 gene specific protein with physical phenotype of fragile X males and females in pedigrees: A new perspective | 0 | 3 |
| 1270 | 15 | 39 | 2233 2003 AMERICAN JOURNAL ON MENTAL RETARDATION 108(3):149-160 Abbeduto L; Murphy MM; Cawthon SW; Richmond EK; Weissman MD; Karadottir S; O'Brien A Receptive language skills of adolescents and young adults with Down or fragile X syndrome | 2 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1271 | 9 | 26 | 2245 2003 BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 305(2):434-441 Dolzhanskaya N; Sung YJ; Conti J; Currie JR; Denman RB The fragile X mental retardation protein interacts with U-rich RNAs in a yeast three-hybrid system | 2 | 3 |
| 1272 | 26 | 40 | 2246 2003 BIOCHEMISTRY 42(35):10437-10444 Adinolfi S; Ramos A; Martin SR; Dal Piaz F; Pucci P; Bardoni B; Mandel JL; Pastore A The N-terminus of the fragile X mental retardation protein contains a novel domain involved in dimerization and RNA binding | 2 | 3 |
| 1273 | 4 | 6 | 2254 2003 CLINICAL GENETICS 64(1):54-56 Rogers C; Partington MW; Turner GM Tremor, ataxia and dementia in older men may indicate a carrier of the fragile X syndrome | 3 | 3 |
| 1274 | 18 | 33 | 2260 2003 CYTOGENETIC AND GENOME RESEARCH 100(1-4):206-212 Hagerman PJ; Greco CM; Hagerman RJ A cerebellar tremor/ataxia syndrome among fragile X premutation carriers | 2 | 3 |
| 1275 | 22 | 62 | 2261 2003 DEVELOPMENT 130(22):5543-5552 Lee A; Li WJ; Xu KY; Bogert BA; Su K; Gao FB Control of dendritic development by the Drosophila fragile X-related gene involves the small GTPase Rac1 | 2 | 3 |
| 1276 | 36 | 53 | 2271 2003 HUMAN MOLECULAR GENETICS 12(14):1689-1698 Bardoni B; Castets M; Huot ME; Schenck A; Adinolfi S; Corbin F; Pastore A; Khandjian EW; Mandel JL 82-FIP, a novel FMRP (Fragile X Mental Retardation Protein) interacting protein, shows a cell cycle-dependent intracellular localization | 3 | 3 |
| 1277 | 18 | 22 | 2283 2003 JOURNAL OF MEDICAL GENETICS 40(5):377-379 Willemsen R; Smits A; Severijnen LA; Jansen M; Jacobs A; De Bruyn E; Oostra B Predictive testing for cognitive functioning in female carriers of the fragile X syndrome using hair root analysis | 3 | 3 |
| 1278 | 21 | 39 | 2300 2003 NEUROSCIENCE 120(4):1005-1017 Chen L; Yun SW; Seto J; Liu W; Toth M The fragile X mental retardation protein binds and regulates a novel class of mRNAs containing U rich target sequences | 3 | 3 |
| 1279 | 16 | 50 | 2301 2003 NUCLEIC ACIDS RESEARCH 31(14):3963-3970 Weisman-Shomer P; Cohen E; Hershco I; Khateb S; Wolfovitz-Barchad O; Hurley LH; Fry M The cationic porphyrin TMPyP4 destabilizes the tetraplex form of the fragile X syndrome expanded sequence d(CGG)(n) | 2 | 3 |
| 1280 | 21 | 55 | 2332 2004 JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION 291(4):460-469 Jacquemont S; Hagerman RJ; Leehey MA; Hall DA; Levine RA; Brunberg JA; Zhang L; Jardini T; Gane LW; Harris SW; Herman K; Grigsby J; Greco CM; Berry-Kravis E; Tassone F; Hagerman PJ Penetrance of the fragile X - Associated tremor/ataxia syndrome in a premutation carrier population | 3 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1281 | 0 | 0 | 2 1980 AMERICAN JOURNAL OF HUMAN GENETICS 32(6):A114-A114 KAISERMCCAW B; HECHT F THE FRAGILE-X - NO DYSMORPHIC SYNDROME, BUT A MARKER | 2 | 2 |
| 1282 | 0 | 0 | 4 1980 ARIZONA MEDICINE 37(11):764-766 HECHT F; KAISERMCCAW B; MOORE BC; CADIEN J; GLOVER TW THE FRAGILE X-CHROMOSOME MENTAL-RETARDATION AND LARGE TESTES | 2 | 2 |
| 1283 | 0 | 0 | 54 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 |
| 1284 | 0 | 0 | 71 1982 JOURNAL OF MEDICAL GENETICS 19(1):64-64 DAKER MG; CHIDIAC P; FEAR CN; BERRY AC FRAGILE X-CHROMOSOME IN BROTHERS WITH NORMAL INTELLIGENCE, OR THE MAN WHO MIGHT HAVE BEEN A GENIUS | 0 | 2 |
| 1285 | 0 | 0 | 79 1982 NEUROLOGY 32(4):A190-A190 ROSENBERGER PB; WILSONCIAMBRONE S; MILUNSKY A SPEECH FLUENCY DISORDER IN THE FRAGILE-X SYNDROME | 2 | 2 |
| 1286 | 0 | 1 | 92 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A122-A122 WILSON DP; CARPENTER NJ; BERKOVITZ GD; BROWN TR; MIGEON CJ THYROID-FUNCTION IN FRAGILE X-LINKED MENTAL-RETARDATION | 2 | 2 |
| 1287 | 0 | 0 | 93 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A127-A127 BRYANT EM; GLADSTONE P; MARTIN GM EXPRESSION OF THE FRAGILE-X IN MOUSE-X HUMAN SOMATIC-CELL HYBRIDS | 2 | 2 |
| 1288 | 0 | 0 | 99 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 |
| 1289 | 0 | 0 | 100 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A159-A159 WANG JC; BEARDSLEY GP; ERBE RW THYMIDYLATE METABOLISM AND URACIL MISINCORPORATION IN FRAGILE-X SYNDROME CELLS | 0 | 2 |
| 1290 | 1 | 1 | 107 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1291 | 0 | 0 | 119 1983 CLINICAL GENETICS 23(3):232-232 VANDERHAGEN CB; ORSTAVIK KH; BAKKE J; BERG K MONOZYGOUS MALE TRIPLETS WITH MENTAL-RETARDATION AND A FRAGILE X-CHROMOSOME | 2 | 2 |
| 1292 | 0 | 0 | 123 1983 CLINICAL GENETICS 23(3):254-254 VEENEMA H; GERAEDTS JPM THE FRAGILE-X CHROMOSOME SEGREGATING IN A LARGE PEDIGREE | 2 | 2 |
| 1293 | 0 | 0 | 124 1983 CLINICAL GENETICS 23(3):255-255 VERSCHRAEGENSPAE MR; VANDENBOSSCHE H; MATTON MT APPROACH TO RELATIVES IN FRAGILE X-LINKED MENTAL-RETARDATION | 0 | 2 |
| 1294 | 0 | 0 | 131 1983 CLINICAL RESEARCH 31(2):A290-A290 BRANDA RF; ARTHUR DC; KING RA FRAGILE X PATIENTS HAVE NORMAL FOLATE METABOLISM | 2 | 2 |
| 1295 | 2 | 6 | 155 1983 NEW ENGLAND JOURNAL OF MEDICINE 308(23):1424-1424 HAGERMAN RJ; LEVITAS A DILANTIN AND THE FRAGILE X-SYNDROME | 0 | 2 |
| 1296 | 0 | 0 | 162 1983 TERATOLOGY 28(1):A30-A30 ISHIKIRIYAMA S; NIIKAWA N 2 JAPANESE PATIENTS WITH FRAGILE X SYNDROME | 0 | 2 |
| 1297 | 5 | 15 | 165 1984 ALABAMA JOURNAL OF MEDICAL SCIENCES 21(3):284-286 MIXON JC; DEV VG UNDERSTANDING THE FRAGILE X-SYNDROME | 0 | 2 |
| 1298 | 0 | 1 | 202 1984 HUMAN GENETICS 66(1):100-100 GARDNER RJM FRAGILE-X HOMOZYGOSITY DUE TO SOMATIC CROSSING-OVER | 1 | 2 |
| 1299 | 5 | 14 | 265 1985 CLINICAL GENETICS 27(6):529-534 WEBB TP CO-CULTIVATION STUDIES IN THE EXPRESSION OF FRAGILE(X) (Q27) IN LYMPHOCYTES | 1 | 2 |
| 1300 | 0 | 5 | 273 1985 CYTOGENETICS AND CELL GENETICS 40(1-4):653-653 HOLDEN JJA; MULLIGAN LM; FORSTERGIBSON C; SIMPSON NE; WHITE BN; OBERLE I; WROGEMANN K APPLICATION OF FLANKING DNA PROBES TO CARRIER DETECTION IN THE FRAGILE-X SYNDROME | 0 | 2 |
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