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Nodes: 2369
Authors: 4634,
Journals: 373,
Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by first author.
Page 13: 1 (Abbeduto L) 2 (BELGHITI D) 3 (Brown WT) 4 (Chen X) 5 (DAKER MG) 6 (DYKENS E) 7 (FITCHETT M) 8 (GLOVER TW) 9 (HAGERMAN RJ) 10 (HOFFMAN M) 11 (JANCAR J) 12 (KIMCHISARFATY C) 13 (LEE JT) 14 (MAES B) 15 (MIGEON BR) 16 (Myers GF) 17 (Patsalis PC) 18 (REISS AL) 19 (Schenck A) 20 (SMITS APT) 21 (SZABO P) 22 (TURNER G) 23 (Wang YC) 24 (WOHRLE D)
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 1201 | 0 | 0 | 776 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):383-383 LEE JT; MURGIA A; WARREN S; NELSON D; NUSSBAUM R CONSTRUCTION OF A 600-KB YAC CONTIG PROXIMAL TO THE FRAGILE X-SITE | 0 | 0 |
| 1202 | 1 | 16 | 1205 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 |
| 1203 | 0 | 0 | 2356 2004 MOVEMENT DISORDERS 19:S338-S338 Leehey MA; Berry-Kravis E; Jacquemont S; Zhang L; Hagerman R; Hagerman PJ Misdiagnosis of fragile X associated tremor/ataxia syndrome (FXTAS) | 0 | 0 |
| 1204 | 0 | 0 | 2182 2002 NEUROLOGY 58(7):A481-A482 Leehey MA; Brunberg JA; Lang AE; Jacquemont S; Rubinstein D; Greco C; Grigsby J; Tassone F; Hagerman R; Hagerman PJ MRI increased T2 signal intensity in the cerebellar peduncles: Specific for the fragile X premutation tremor/ataxia syndrome? | 0 | 0 |
| 1205 | 0 | 0 | 2174 2002 MOVEMENT DISORDERS 17:S351-S351 Leehey MA; Grigsby J; Rubinstein D; Jacquemont S; Greco C; Zhang L Parkinsonism, tremor and ataxia in a female fragile X carrier | 1 | 1 |
| 1206 | 13 | 30 | 2242 2003 ARCHIVES OF NEUROLOGY 60(1):117-121 Leehey MA; Munhoz RP; Lang AE; Brunberg JA; Grigsby J; Greco C; Jacquemont S; Tassone F; Lozano AM; Hagerman PJ; Hagerman RJ The fragile X premutation presenting as essential tremor | 6 | 13 |
| 1207 | 0 | 0 | 2357 2004 MOVEMENT DISORDERS 19:S339-S339 Leehey MA; Zhang L; Wheelock V; Tassone F; Hagerman R; Hagerman P A preliminary observation: Increased frequency of fragile X expanded alleles in patients that meet diagnostic criteria for MSA | 0 | 0 |
| 1208 | 0 | 0 | 503 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):22-22 LEISTI J; KAHKONEN M; HERVA R; WINQVIST R; UKKOLA L; HEINO R; VAISANEN ML; REKILA A; LINNA SL THE FRAGILE-X SYNDROME IN NORTHERN FINLAND - A GENEALOGIC STUDY | 0 | 0 |
| 1209 | 0 | 0 | 11 1981 BULLETIN DE L ACADEMIE NATIONALE DE MEDECINE 165(9):1197-1206 LEJEUNE J MONOCARBONS METABOLISM AND FRAGILE-X SYNDROME | 22 | 30 |
| 1210 | 4 | 9 | 77 1982 LANCET 1(8266):273-274 LEJEUNE J IS THE FRAGILE-X SYNDROME AMENABLE TO TREATMENT | 46 | 61 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1211 | 0 | 2 | 49 1982 ANNALES DE GENETIQUE 25(3):149-151 LEJEUNE J; LEGRAND N; LAFOURCADE J; RETHORE MO; RAOUL O; MAUNOURY C THE FRAGILE X - EFFECT OF TRIMETHOPRIME TREATMENT | 15 | 24 |
| 1212 | 4 | 11 | 189 1984 ANNALES DE GENETIQUE 27(4):230-232 LEJEUNE J; RETHORE MO; DEBLOIS MC; RAVEL A ASSAY OF FOLIC-ACID TREATMENT IN FRAGILE-X SYNDROME | 7 | 12 |
| 1213 | 4 | 11 | 309 1985 SEMAINE DES HOPITAUX 61(25):1807-1809 LEJEUNE J; RETHORE MO; DEBLOIS MC; RAVEL A ASSAY OF FOLIC-ACID TREATMENT IN FRAGILE-X SYNDROME | 0 | 0 |
| 1214 | 38 | 83 | 625 1989 ARCHIVES FRANCAISES DE PEDIATRIE 46(3):211-216 LELOUARN P; MORAINE C; PERROT A; BARTHELEMY C; GARREAU B; SAUVAGE D AUTISM AND FRAGILE X-SYNDROME | 3 | 5 |
| 1215 | 0 | 1 | 115 1983 BIOLOGY OF THE CELL 48(2-3):A92-A92 LENOARD C; SCHOEVAERT D; SELVA J APPLICATION OF THE AUTOMATIC-ANALYSIS OF METAPHASES TO THE DIAGNOSIS OF THE FRAGILE-X IN MAN | 0 | 0 |
| 1216 | 5 | 24 | 1360 1995 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 25(6):655-662 Lenti C; Peruzzi C; Bianchini E The association between autism and fragile X syndrome: A case report | 0 | 1 |
| 1217 | 0 | 0 | 1768 1999 ARCHIVES OF CLINICAL NEUROPSYCHOLOGY 14(8):767-767 Lesniak-Karpiak K; Mazzocco MM; Lanham DC; Denckla MB Behavioral assessment of social skills in children with Turner syndrome or Fragile X. | 0 | 0 |
| 1218 | 20 | 54 | 2275 2003 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 33(1):55-67 Lesniak-Karpiak K; Mazzocco MMM; Ross JL Behavioral assessment of social anxiety in females with Turner or fragile X syndrome | 0 | 1 |
| 1219 | 10 | 11 | 1202 1994 ARCHIVES OF PEDIATRICS & ADOLESCENT MEDICINE 148(1):63-64 LEUNG AKC; MCLEOD DR; ROBSON WLM; FAGAN JE PICTURE OF THE MONTH - FRAGILE-X SYNDROME | 0 | 1 |
| 1220 | 12 | 21 | 1192 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):527-534 LEVINSON G; MADDALENA A; PALMER FT; HARTON GL; BICK DP; HOWARDPEEBLES PN; BLACK SH; SCHULMAN JD IMPROVED SIZING OF FRAGILE-X CCG REPEATS BY NESTED POLYMERASE CHAIN-REACTION | 15 | 28 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1221 | 1 | 5 | 1940 2000 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 39(4):398-398 Levitas A Fragile X syndrome | 0 | 0 |
| 1222 | 7 | 20 | 142 1983 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 4(3):151-158 LEVITAS A; HAGERMAN RJ; BRADEN M; RIMLAND B; MCBOGG P; MATUS I AUTISM AND THE FRAGILE-X SYNDROME | 48 | 62 |
| 1223 | 11 | 59 | 1876 2000 CELL 100(3):323-332 Lewis HA; Musunuru K; Jensen KB; Edo C; Chen H; Darnell RB; Burley SK Sequence-specific RNA binding by a Nova KH domain: Implications for paraneoplastic disease and the fragile X syndrome | 7 | 86 |
| 1224 | 22 | 75 | 2172 2002 MOLECULAR AND CELLULAR NEUROSCIENCE 19(2):138-151 Li JX; Pelletier MR; Velazquez JLP; Carlen PL Reduced cortical synaptic plasticity and GluR1 expression associated with fragile X mental retardation protein deficiency | 9 | 13 |
| 1225 | 0 | 0 | 1837 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):57-57 Li MM; Nelson L; Bamshad M; Ward K Fragile X mosaics in a family with multiple mildly affected individuals. | 0 | 0 |
| 1226 | 0 | 0 | 755 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):235-235 LI Q; XU DD; ZHOU LY FRAGILE X-FREQUENCY IN MENTALLY-RETARDED CHILDREN AND IN FETAL BLOOD BY CORDOCENTESIS | 0 | 0 |
| 1227 | 8 | 33 | 704 1990 HUMAN GENETICS 85(3):267-271 LI SY; LIN JK DIFFERENTIAL BLEOMYCIN SUSCEPTIBILITY IN CULTURED LYMPHOCYTES OF FRAGILE X-PATIENTS AND NORMAL INDIVIDUALS | 3 | 5 |
| 1228 | 4 | 30 | 587 1988 HUMAN GENETICS 79(4):292-296 LI SY; TSAI CC; CHOU MY; LIN JK A CYTOGENETIC STUDY OF MENTALLY-RETARDED SCHOOL-CHILDREN IN TAIWAN WITH SPECIAL REFERENCE TO THE FRAGILE X-CHROMOSOME | 6 | 17 |
| 1229 | 18 | 36 | 2051 2001 NUCLEIC ACIDS RESEARCH 29(11):2276-2283 Li ZZ; Zhang YY; Ku L; Wilkinson KD; Warren ST; Feng Y The fragile X mental retardation protein inhibits translation via interacting with mRNA | 46 | 67 |
| 1230 | 0 | 0 | 1691 1998 MOLECULAR BIOLOGY OF THE CELL 9:185A-185A Lichtenstein H; Tartakoff A Nuclear export of the Fragile X gene product, FMRP | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1231 | 23 | 46 | 1145 1993 PSYCHIATRIE DE L ENFANT 36(1):5-26 LIDAPULIK H; BASQUIN M COGNITIVE DISTURBANCES AND PSYCHIATRIC MANIFESTATIONS IN THE FRAGILE-X SYNDROME - AUTISM AND FRAGILE-X SYNDROME | 0 | 1 |
| 1232 | 4 | 9 | 1861 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 95(5):516-517 Limprasert P; Jaruratanasirikul S; Vasiknanonte P Unilateral macroorchidism in fragile X syndrome | 2 | 2 |
| 1233 | 0 | 7 | 1338 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):359-362 Lin JFH Introduction to fragile X syndrome for parents | 0 | 0 |
| 1234 | 12 | 23 | 439 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 |
| 1235 | 10 | 22 | 1735 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):318-321 Linden MG; Tassone F; Gane LW; Hills JL; Hagerman RJ; Taylor AK Compound heterozygous female with fragile X syndrome | 0 | 1 |
| 1236 | 0 | 4 | 223 1984 LANCET 1(8370):220-221 LINNA SL; SIMILA S; HARO E; HERVA R PREVALENCE OF FRAGILE X-CHROMOSOME | 2 | 4 |
| 1237 | 6 | 13 | 1880 2000 CLINICAL GENETICS 57(6):456-458 Lisik M The comparison of anthropometric variables in mentally retarded boys with and without fragile X syndrome | 0 | 0 |
| 1238 | 13 | 56 | 1470 1996 COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY 61:689-697 Liu Q; Siomi H; Siomi MC; Fischer U; Zhang Y; Wan L; Dreyfuss G Molecular characterization of the protein products of the fragile X syndrome gene and the survival of motor neurons gene | 2 | 10 |
| 1239 | 2 | 11 | 1257 1994 THERIOGENOLOGY 42(5):789-794 LLAMBI S; POSTIGLIONI A LOCALIZATION OF THE FRAGILE-X CHROMOSOME BREAK POINTS IN HOLSTEIN-FRIESIAN CATTLE (BOS-TAURUS) | 0 | 2 |
| 1240 | 0 | 0 | 380 1986 CLINICAL RESEARCH 34(1):A114-A114 LOEHR JP; SYNHORST DP; HAGERMAN RJ; WOLFE RR CARDIOVASCULAR-ABNORMALITIES IN THE FRAGILE-X SYNDROME | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1241 | 3 | 18 | 322 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):189-194 LOEHR JP; SYNHORST DP; WOLFE RR; HAGERMAN RJ AORTIC ROOT DILATATION AND MITRAL-VALVE PROLAPSE IN THE FRAGILE-X SYNDROME | 19 | 28 |
| 1242 | 9 | 31 | 359 1986 ANNALS OF HUMAN GENETICS 50:385-398 LOESCH DZ DERMATOGLYPHIC FINDINGS IN FRAGILE X-SYNDROME - A CAUSAL HYPOTHESIS POINTS TO X-Y INTERCHANGE | 9 | 14 |
| 1243 | 0 | 0 | 425 1987 AUSTRALIAN PAEDIATRIC JOURNAL 23(1):75-75 LOESCH DZ DERMATOGLYPHIC ABNORMALITY IN FRAGILE X-SYNDROME - A NEW CAUSAL HYPOTHESIS | 0 | 0 |
| 1244 | 1 | 22 | 438 1987 COLLEGIUM ANTROPOLOGICUM 11(2):305-316 LOESCH DZ FACTOR-ANALYSIS OF RIDGE-PATTERNS AND HAND MEASUREMENTS IN NORMAL AND FRAGILE-X MALES | 0 | 2 |
| 1245 | 6 | 13 | 570 1988 CLINICAL GENETICS 33(3):169-175 LOESCH DZ DISCRIMINANT-ANALYSIS OF DERMATOGLYPHIC MEASUREMENTS IN FRAGILE-X MALES AND FEMALES | 0 | 1 |
| 1246 | 12 | 20 | 1445 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):413-414 Loesch DZ Fragile X: Clinical associations | 0 | 0 |
| 1247 | 1 | 2 | 1610 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 |
| 1248 | 0 | 0 | 2124 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:220-220 Loesch DZ Effect of prennutation in the FMR1 gene on cognitive and physical phenotype in fragile X assessed by pedigree analysis. | 0 | 0 |
| 1249 | 41 | 101 | 2298 2003 NEUROPSYCHOLOGY 17(4):646-657 Loesch DZ; Bui QM; Grigsby J; Butler E; Epstein J; Huggins RM; Taylor AK; Hagerman RJ Effect of the fragile X status categories and the fragile X mental retardation protein levels on executive functioning in males and females with fragile X | 1 | 1 |
| 1250 | 0 | 0 | 365 1986 AUSTRALIAN PAEDIATRIC JOURNAL 22(4):350-350 LOESCH DZ; HAY D PHENOTYPIC DIVERSITY OF FRAGILE-X FEMALES AND ITS GENETIC-IMPLICATIONS | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1251 | 5 | 17 | 605 1988 JOURNAL OF MEDICAL GENETICS 25(6):407-414 LOESCH DZ; HAY DA CLINICAL-FEATURES AND REPRODUCTIVE PATTERNS IN FRAGILE-X FEMALE HETEROZYGOTES | 33 | 43 |
| 1252 | 9 | 24 | 1169 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):392-399 LOESCH DZ; HAY DA; MULLEY J TRANSMITTING MALES AND CARRIER FEMALES IN FRAGILE-X - REVISITED | 21 | 31 |
| 1253 | 5 | 25 | 953 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 44(5):543-550 LOESCH DZ; HAY DA; SHEFFIELD LJ FRAGILE-X FAMILY WITH UNUSUAL DIGITAL AND FACIAL ABNORMALITIES, CLEFT-LIP AND PALATE, AND EPILEPSY | 8 | 12 |
| 1254 | 12 | 29 | 416 1987 AMERICAN JOURNAL OF MEDICAL GENETICS 27(2):401-417 LOESCH DZ; HAY DA; SUTHERLAND GR; HALLIDAY J; JUDGE C; WEBB GC PHENOTYPIC VARIATION IN MALE-TRANSMITTED FRAGILE-X - GENETIC INFERENCES | 36 | 51 |
| 1255 | 0 | 0 | 779 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):474-474 LOESCH DZ; HUGGINS R ESTIMATION OF THE EFFECTS OF FRAGILE-X ON DISTRIBUTIONS OF PHYSICAL AND INTELLECTUAL MEASURES USING A MAXIMUM-LIKELIHOOD SCORING TECHNIQUE | 0 | 0 |
| 1256 | 17 | 35 | 1057 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(5):1064-1073 LOESCH DZ; HUGGINS R; HAY DA; GEDEON AK; MULLEY JC; SUTHERLAND GR GENOTYPE-PHENOTYPE RELATIONSHIPS IN FRAGILE-X SYNDROME - A FAMILY STUDY | 43 | 60 |
| 1257 | 0 | 0 | 1070 1993 BEHAVIOR GENETICS 23(6):557-557 LOESCH DZ; HUGGINS R; HAY DA; GODEON AK; MULLEY JC; SUTHERLAND GR GENOTYPE-PHENOTYPE RELATIONSHIPS IN FRAGILE-X - A FAMILY STUDY | 0 | 0 |
| 1258 | 20 | 27 | 1292 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(6):1408-1413 LOESCH DZ; HUGGINS R; PETROVIC V; SLATER H EXPANSION OF THE CGG REPEAT IN FRAGILE-X IN THE FMR1 GENE DEPENDS ON THE SEX OF THE OFFSPRING | 5 | 12 |
| 1259 | 5 | 29 | 902 1992 AMERICAN JOURNAL OF HUMAN GENETICS 50(5):1067-1076 LOESCH DZ; HUGGINS RM FIXED AND RANDOM EFFECTS IN THE VARIATION OF THE FINGER RIDGE COUNT - A STUDY OF FRAGILE-X FAMILIES | 7 | 8 |
| 1260 | 32 | 51 | 2152 2002 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 23(6):416-423 Loesch DZ; Huggins RM; Bui QM; Epstein JL; Taylor AK; Hagerman RJ Effect of the deficits of fragile X mental retardation protein on cognitive status of fragile X males and females assessed by robust pedigree analysis | 5 | 5 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1261 | 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 |
| 1262 | 35 | 62 | 2228 2003 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 122A(1):13-23 Loesch DZ; Huggins RM; Bui QM; Taylor AK; Pratt C; Epstein J; Hagerman RJ Effect of fragile x status categories and FMRP deficits on cognitive profiles estimated by robust pedigree analysis | 0 | 1 |
| 1263 | 6 | 26 | 1061 1993 AMERICAN JOURNAL OF MEDICAL GENETICS 46(4):415-422 LOESCH DZ; HUGGINS RM; CHIN WF EFFECT OF FRAGILE-X ON PHYSICAL AND INTELLECTUAL TRAITS ESTIMATED BY PEDIGREE ANALYSIS | 7 | 9 |
| 1264 | 38 | 66 | 2347 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):31-41 Loesch DZ; Huggins RM; Hagerman RJ Phenotypic variation and FMRP levels in fragile X | 0 | 0 |
| 1265 | 16 | 33 | 1296 1995 AMERICAN JOURNAL OF MEDICAL GENETICS 58(3):249-256 LOESCH DZ; HUGGINS RM; HOANG NH GROWTH IN STATURE IN FRAGILE-X FAMILIES - A MIXED LONGITUDINAL-STUDY | 12 | 14 |
| 1266 | 9 | 18 | 2094 2002 AMERICAN JOURNAL OF MEDICAL GENETICS 107(2):136-142 Loesch DZ; Huggins RM; Taylor AK Application of robust pedigree analysis in studies of complex genotype-phenotype relationships in fragile X syndrome | 5 | 6 |
| 1267 | 18 | 26 | 1575 1997 CLINICAL GENETICS 51(1):1-6 Loesch DZ; Petrovic V; Francis DI; Oertel R; Slater H ''Reduction'' of CGG trinucleotide expansion from mother to offspring in seven fragile-X families | 4 | 7 |
| 1268 | 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 |
| 1269 | 14 | 31 | 1093 1993 HUMAN GENETICS 91(5):469-474 LOESCH DZ; SHEFFIELD LJ; HAY DA BETWEEN-GENERATION DIFFERENCES IN ASCERTAINMENT AND PENETRANCE - RELEVANCE TO GENETIC HYPOTHESES IN FRAGILE-X | 5 | 5 |
| 1270 | 5 | 19 | 617 1989 AMERICAN JOURNAL OF MEDICAL GENETICS 33(2):200-208 LOESCH DZ; WILSON SR MULTIVARIATE-ANALYSIS OF BODY SHAPE IN FRAGILE-X (MARTIN-BELL) SYNDROME | 2 | 5 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1271 | 0 | 0 | 767 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):291-291 LOGHINGROSSO NS; LAUANDOS JE; ALI VRA; GRACA CHN; SCHMIDT BJ SEARCHING FOR FRAGILE-X IN AN INSTITUTION FOR MENTALLY-HANDICAPPED IN BRAZIL | 0 | 0 |
| 1272 | 0 | 5 | 1941 2000 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 39(4):398-399 Lombroso PJ Fragile X syndrome - Dr. Lombroso replies | 0 | 0 |
| 1273 | 8 | 10 | 2288 2003 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 42(3):372-375 Lombroso PJ Genetics of childhood disorders: XLVIII. Learning and memory, part 1: Fragile X syndrome update | 0 | 0 |
| 1274 | 6 | 7 | 1210 1994 CLINICAL GENETICS 45(4):186-189 LOPEZPAJARES I; DELICADO A; PASCUALCASTROVIEJO I; LOPEZMARTIN V; MORENO F; GARCIAMARCOS JA FRAGILE-X SYNDROME WITH EXTRA MICROCHROMOSOME | 0 | 1 |
| 1275 | 10 | 15 | 1612 1997 JOURNAL OF MEDICAL GENETICS 34(11):924-926 Losekoot M; Hoogendoorn E; Olmer R; Jansen CCAM; Oosterwijk JC; vandenOuweland AMW; Halley DJJ; Warren ST; Willemsen R; Oostra BA; Bakker E 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 |
| 1276 | 0 | 0 | 759 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):269-269 LOZZIO CB; MATTESON K; CACHEIRO NL CARRIER DETECTION OF FRAGILE-X USING TRIMETHOPRIM AND DNA LINKAGE ANALYSES | 0 | 0 |
| 1277 | 8 | 13 | 686 1990 ANNALES DE GENETIQUE 33(2):109-110 LUCOTTE G A NEW DNA PROBE OF POTENTIAL USE FOR DIAGNOSIS OF THE FRAGILE-X SYNDROME | 0 | 0 |
| 1278 | 15 | 24 | 1381 1995 NATURE GENETICS 10(4):483-485 LUGENBEEL KA; PEIER AM; CARSON NL; CHUDLEY AE; NELSON DL INTRAGENIC LOSS OF FUNCTION MUTATIONS DEMONSTRATE THE PRIMARY ROLE OF FMR1 IN FRAGILE-X SYNDROME | 30 | 49 |
| 1279 | 2 | 5 | 2289 2003 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 42(5):516-517 Lung FW; Chen PJ Fragile X syndrome in adolescent prostitutes in southern Taiwan | 0 | 1 |
| 1280 | 0 | 0 | 1920 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:374-374 Lung FW; Shu BC Fragile-X syndrome in adolescent prostitutes | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1281 | 11 | 27 | 1147 1993 SOMATIC CELL AND MOLECULAR GENETICS 19(4):393-404 LUO SY; ROBINSON JC; REISS AL; MIGEON BR DNA METHYLATION OF THE FRAGILE-X LOCUS IN SOMATIC AND GERM-CELLS DURING FETAL DEVELOPMENT - RELEVANCE TO THE FRAGILE-X SYNDROME AND X-INACTIVATION | 6 | 19 |
| 1282 | 0 | 0 | 1084 1993 CYTOGENETICS AND CELL GENETICS 63(4):252-252 LUTHARDT F; SKOGERBOE K; SHADOAN P; DINNO N IDENTIFICATION OF DE-NOVO DEL(Y)(Q11.23) IN A FRAGILE-X NEGATIVE, MENTALLY-RETARDED MALE USING A Y-CHROMOSOME COCKTAIL PROBE (DYZ1, DYZ3) | 0 | 0 |
| 1283 | 0 | 0 | 854 1991 CYTOGENETICS AND CELL GENETICS 58(3-4):2076-2076 LYNCH M; KREMER EJ; PRITCHARD MA; YU S; BAKER E; NAGARAJA R; HEITZ D; HYLAND VJ; LITTLE RD; WADA M; TONIOLO D; VINCENT A; ROUSSEAU F; NANCARROW J; HOLMAN K; MULLEY JC; WARREN ST; MANDEL J; SCHLESSINGER D; SUTHERLAND GR; RICHARDS RI THE FRAGILE-X GENOTYPE IS CHARACTERIZED BY AN UNSTABLE REGION OF DNA | 0 | 0 |
| 1284 | 0 | 0 | 1104 1993 IRISH MEDICAL JOURNAL 86(5):172-172 LYNCH SA FRAGILE-X SYNDROME | 0 | 0 |
| 1285 | 6 | 24 | 673 1990 AMERICAN JOURNAL OF HUMAN GENETICS 47(2):181-187 MACKINNON RN; HIRST MC; BELL MV; WATSON JEV; CLAUSSEN U; LUDECKE HJ; SENGER G; HORSTHEMKE B; DAVIES KE MICRODISSECTION OF THE FRAGILE-X REGION | 9 | 37 |
| 1286 | 7 | 11 | 950 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(5):905-912 MACPHERSON J; HARVEY J; CURTIS G; WEBB T; HEITZ D; ROUSSEAU F; JACOBS P A REINVESTIGATION OF 33 FRAGILE(X) FAMILIES USING PROBE STB12.3 | 7 | 9 |
| 1287 | 2 | 5 | 1806 1999 JOURNAL OF MEDICAL GENETICS 36(2):171-171 Macpherson J; Murray A; Webb J; Jacobs P Fragile X syndrome: of POF and premutations | 0 | 1 |
| 1288 | 1 | 4 | 2269 2003 HUMAN GENETICS 112(5-6):619-620 Macpherson J; Waghorn A; Hammans S; Jacobs P Observation of an excess of fragile-X premutations in a population of males referred with spinocerebellar ataxia | 5 | 6 |
| 1289 | 20 | 28 | 1219 1994 HUMAN MOLECULAR GENETICS 3(3):399-405 MACPHERSON JN; BULLMAN H; YOUINGS SA; JACOBS PA INSERT SIZE AND FLANKING HAPLOTYPE IN FRAGILE-X AND NORMAL-POPULATIONS - POSSIBLE MULTIPLE ORIGINS FOR THE FRAGILE-X MUTATION | 28 | 57 |
| 1290 | 16 | 27 | 1372 1995 JOURNAL OF MEDICAL GENETICS 32(3):236-239 MACPHERSON JN; CURTIS G; CROLLA JA; DENNIS N; MIGEON B; GREWAL PK; HIRST MC; DAVIES KE; JACOBS PA UNUSUAL (CGG)(N) EXPANSION AND RECOMBINATION IN A FAMILY WITH FRAGILE-X AND DIGEORGE-SYNDROME | 3 | 11 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1291 | 17 | 18 | 1186 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):490-496 MADDALENA A; HICKS BD; SPENCE WC; LEVINSON G; HOWARDPEEBLES PN PRENATAL-DIAGNOSIS IN KNOWN FRAGILE-X CARRIERS | 7 | 12 |
| 1292 | 0 | 0 | 1031 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):88-88 MADDALENA A; SPENCE WC; LEVINSON G; HOWARDPEEBLES PN FRAGILE-X PRENATAL-DIAGNOSIS IN KNOWN CARRIERS | 0 | 0 |
| 1293 | 18 | 21 | 1429 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):309-312 Maddalena A; Yadvish KN; Spence WC; HowardPeebles PN A fragile X mosaic male with a cryptic full mutation detected in epithelium but not in blood | 12 | 15 |
| 1294 | 6 | 45 | 397 1986 JOURNAL OF MENTAL DEFICIENCY RESEARCH 30:129-148 MADISON LS; GEORGE C; MOESCHLER JB COGNITIVE-FUNCTIONING IN THE FRAGILE-X SYNDROME - A STUDY OF INTELLECTUAL, MEMORY AND COMMUNICATION-SKILLS | 24 | 29 |
| 1295 | 14 | 52 | 398 1986 JOURNAL OF PEDIATRIC PSYCHOLOGY 11(1):91-102 MADISON LS; MOSHER GA; GEORGE CH FRAGILE-X SYNDROME - DIAGNOSIS AND RESEARCH | 0 | 12 |
| 1296 | 8 | 18 | 390 1986 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 7(4):253-256 MADISON LS; WELLS TE; FRISTO TE; BENESCH CG A CONTROLLED-STUDY OF FOLIC-ACID TREATMENT IN 3 FRAGILE-X SYNDROME MALES | 5 | 6 |
| 1297 | 0 | 0 | 1401 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):6-6 Maes B; Borghraef M; Fryns JP Presentation of a fragile-X screening list. | 0 | 0 |
| 1298 | 22 | 29 | 1944 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 |
| 1299 | 38 | 84 | 1090 1993 GENETIC COUNSELING 4(4):245-263 MAES B; FRYNS JP; VANWALLEGHEM M; VANDENBERGHE H FRAGILE-X SYNDROME AND AUTISM - A PREVALENT ASSOCIATION OR A MISINTERPRETED CONNECTION | 6 | 13 |
| 1300 | 28 | 64 | 1152 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 50(2):190-200 MAES B; FRYNS JP; VANWALLEGHEM M; VANDENBERGHE H COGNITIVE-FUNCTIONING AND INFORMATION-PROCESSING OF ADULT MENTALLY-RETARDED MEN WITH FRAGILE-X SYNDROME | 17 | 24 |
Page 13: 1 (Abbeduto L) 2 (BELGHITI D) 3 (Brown WT) 4 (Chen X) 5 (DAKER MG) 6 (DYKENS E) 7 (FITCHETT M) 8 (GLOVER TW) 9 (HAGERMAN RJ) 10 (HOFFMAN M) 11 (JANCAR J) 12 (KIMCHISARFATY C) 13 (LEE JT) 14 (MAES B) 15 (MIGEON BR) 16 (Myers GF) 17 (Patsalis PC) 18 (REISS AL) 19 (Schenck A) 20 (SMITS APT) 21 (SZABO P) 22 (TURNER G) 23 (Wang YC) 24 (WOHRLE D)
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