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Nodes: 2369
Authors: 4634,
Journals: 373,
Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by first author.
Page 22: 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 |
|---|---|---|---|---|---|
| 2101 | 0 | 1 | 486 1987 NEW ENGLAND JOURNAL OF MEDICINE 316(8):483-483 TURNER G THE FRAGILE X-CHROMOSOME - REPLY | 1 | 1 |
| 2102 | 0 | 0 | 562 1988 AUSTRALIAN PAEDIATRIC JOURNAL 24(1):91-91 TURNER G ISSUES ARISING FROM FRAGILE-X PREVENTIVE SCREENING | 0 | 0 |
| 2103 | 0 | 0 | 740 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):35-35 TURNER G FRAGILE X-SYNDROME | 0 | 0 |
| 2104 | 0 | 0 | 364 1986 AUSTRALIAN PAEDIATRIC JOURNAL 22(3):237-237 TURNER G; LAING S; ROBINSON H; PURVISSMITH S A PROGRAM FOR PRIMARY PREVENTION OF INTELLECTUAL HANDICAP - FRAGILE (X) SCREENING | 0 | 0 |
| 2105 | 1 | 2 | 317 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):11-67 TURNER G; OPITZ JM; BROWN WT; DAVIES KE; JACOBS PA; JENKINS EC; MIKKELSEN M; PARTINGTON MW; SUTHERLAND GR CONFERENCE REPORT - 2ND INTERNATIONAL WORKSHOP ON THE FRAGILE-X AND ON X-LINKED MENTAL-RETARDATION | 51 | 71 |
| 2106 | 1 | 2 | 533 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):423-428 TURNER G; PARTINGTON MW FRAGILE(X) EXPRESSION, AGE AND THE DEGREE OF INTELLECTUAL HANDICAP IN THE MALE | 4 | 5 |
| 2107 | 0 | 0 | 508 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):26-27 TURNER G; PARTINGTON MW; ROBINSON H; LATHAM M; KENNY J; VANDENBERK M; LAING S; THODE A THE PROS AND CONS OF PREVENTIVE SCREENING FOR THE FRAGILE (X) | 0 | 0 |
| 2108 | 1 | 6 | 404 1986 NEW ENGLAND JOURNAL OF MEDICINE 315(10):607-609 TURNER G; ROBINSON H; LAING S; PURVISSMITH S PREVENTIVE SCREENING FOR THE FRAGILE-X SYNDROME | 95 | 123 |
| 2109 | 0 | 0 | 771 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):331-331 TURNER G; ROBINSON H; LAING S; SHERMAN S SCREENING FOR THE FRAGILE X-SYNDROME - IMPACT OF GENETIC-COUNSELING ON REPRODUCTIVE CHOICES OF WOMEN AT RISK FOR HAVING AN AFFECTED CHILD | 0 | 0 |
| 2110 | 6 | 22 | 999 1992 LANCET 339(8803):1210-1213 TURNER G; ROBINSON H; LAING S; VANDENBERK M; COLLEY A; GODDARD A; SHERMAN S; PARTINGTON M POPULATION SCREENING FOR FRAGILE-X | 20 | 38 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2111 | 8 | 10 | 1574 1997 BRITISH MEDICAL JOURNAL 315(7117):1223-1226 Turner G; Robinson H; Wake S; Laing S; Partington M Case finding for the fragile X syndrome and its consequences | 5 | 9 |
| 2112 | 2 | 5 | 1246 1994 LANCET 344(8935):1500-1500 TURNER G; ROBINSON H; WAKE S; MARTIN N DIZYGOUS TWINNING AND PREMATURE MENOPAUSE IN FRAGILE-X SYNDROME | 31 | 50 |
| 2113 | 11 | 12 | 1412 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):196-197 Turner G; Webb T; Wake S; Robinson H Prevalence of fragile X syndrome | 137 | 223 |
| 2114 | 0 | 0 | 2127 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:228-228 Tzeng C; Chen W; Huang K Prevalence of fragile-X female carrier in Taiwan is lower than expected | 0 | 0 |
| 2115 | 16 | 23 | 1781 1999 DIAGNOSTIC MOLECULAR PATHOLOGY 8(3):152-156 Tzeng CC; Cho WC; Kuo PL; Chen RM Pilot fragile X screening in normal population of Taiwan | 7 | 9 |
| 2116 | 11 | 27 | 2015 2001 DIAGNOSTIC MOLECULAR PATHOLOGY 10(1):34-40 Tzeng CC; Lin SJ; Chen YJ; Kuo PL; Jong YJ; Tsai LP; Chen RM An effective strategy of using molecular testing to screen mentally retarded individuals for fragile X syndrome | 1 | 2 |
| 2117 | 0 | 0 | 1926 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:496-497 Tzeng CC; Lin SJ; Chen YY; Chen RM An effective strategy of using a molecular test to screen individuals with mental retardation for fragile-X syndrome | 0 | 0 |
| 2118 | 9 | 16 | 1888 2000 GENETIC TESTING 4(3):235-239 Tzountzouris J; Kennedy D; Skuterud M; Connolly-Wilson M; Holden JJA; Lin CC; Mak-Tam E; Somerville MJ; Summers AM; Allingham-Hawkins DJ Apparently unstable normal FMR1 alleles in nine developmentally delayed patients: Implications for molecular diagnosis of the Fragile X syndrome | 0 | 1 |
| 2119 | 0 | 5 | 346 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):557-562 UCHIDA IA; FREEMAN VCP; BASRUR PK THE FRAGILE-X IN CATTLE | 4 | 20 |
| 2120 | 2 | 13 | 86 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(5):861-868 UCHIDA IA; FREEMAN VCP; JAMRO H; PARTINGTON MW; SOLTAN HC ADDITIONAL EVIDENCE FOR FRAGILE-X ACTIVITY IN HETEROZYGOUS CARRIERS | 25 | 33 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2121 | 0 | 18 | 37 1982 AMERICAN JOURNAL OF HUMAN GENETICS 34(2):286-293 UCHIDA IA; JOYCE EM ACTIVITY OF THE FRAGILE-X IN HETEROZYGOUS CARRIERS | 0 | 66 |
| 2122 | 20 | 59 | 1906 2000 JOURNAL OF BIOLOGICAL CHEMISTRY 275(42):33134-33141 Uliel L; Weisman-Shomer P; Oren-Jazans H; Newcomb T; Loeb LA; Fry M Human Ku antigen tightly binds and stabilizes a tetrahelical form of the fragile X syndrome d(CGG)(n) expanded sequence | 1 | 7 |
| 2123 | 11 | 27 | 1757 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):300-303 Uzielli MLG; Guarducci S; Lapi E; Cecconi A; Ricci U; Ricotti G; Biondi C; Scarselli B; Vieri F; Scarnato P; Gori F; Sereni A Premature ovarian failure (POF) and fragile X premutation females: From POF to fragile X carrier identification, from fragile X carrier diagnosis to POF association data | 11 | 24 |
| 2124 | 15 | 37 | 1397 1996 AMERICAN JOURNAL OF HUMAN GENETICS 59(3):540-546 Vaisanen ML; Haataja R; Leisti L Decrease in the CGG(n) trinucleotide repeat mutation of the fragile X syndrome to normal size range during paternal transmission | 4 | 9 |
| 2125 | 11 | 26 | 941 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):307-311 VAISANEN ML; KAHKONEN M; LEISTI J CARRIER DETECTION OF THE FRAGILE-X SYNDROME WITH FLANKING RFLP MARKERS AND LINKAGE ANALYSIS | 2 | 2 |
| 2126 | 19 | 28 | 1215 1994 HUMAN GENETICS 93(2):143-147 VAISANEN ML; KAHKONEN M; LEISTI J DIAGNOSIS OF FRAGILE-X SYNDROME BY DIRECT MUTATION ANALYSIS | 9 | 12 |
| 2127 | 8 | 32 | 1948 2000 MOLECULAR BRAIN RESEARCH 75(2):337-341 Valentine G; Chakravarty S; Sarvey J; Bramham C; Herkenham M Fragile X (fmr1) mRNA expression is differentially regulated in two adult models of activity-dependent gene expression | 6 | 9 |
| 2128 | 7 | 40 | 1679 1998 JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY AND ALLIED DISCIPLINES 39(5):699-710 van Lieshout CFM; De Meyer RE; Curfs LMG; Fryns JP Family contexts, parental behaviour, and personality profiles of children and adolescents with Prader-Willi, fragile-X, or Williams syndrome | 4 | 16 |
| 2129 | 10 | 48 | 588 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 |
| 2130 | 0 | 0 | 428 1987 BEHAVIOR GENETICS 17(6):642-642 VANDENBERG SG A STATUS-REPORT ON THE FRAGILE X-SYNDROME | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2131 | 16 | 21 | 1184 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):482-485 VANDENOUWELAND AMW; DEVRIES BBA; BAKKER PLG; DEELEN WH; DEGRAAFF E; VANHEMEL JO; OOSTRA BA; NIERMEIJER MF; HALLEY DJJ DNA DIAGNOSIS OF THE FRAGILE-X-SYNDROME IN A SERIES OF 236 MENTALLY-RETARDED SUBJECTS AND EVIDENCE FOR A REVERSAL OF MUTATION IN THE FMR-1 GENE | 26 | 34 |
| 2132 | 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 |
| 2133 | 18 | 55 | 354 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):723-737 VANDYKE DL; WEISS L MATERNAL EFFECT ON INTELLIGENCE IN FRAGILE-X MALES AND FEMALES | 4 | 8 |
| 2134 | 0 | 0 | 379 1986 CLINICAL RESEARCH 34(1):A34-A34 VANDYKE DL; WEISS L MATERNAL EFFECT ON INTELLIGENCE IN FRAGILE-X MALES AND FEMALES - AN HYPOTHESIS | 0 | 0 |
| 2135 | 6 | 18 | 794 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):328-331 VANOOST BA; SMITS A; DREESEN JCFM; SMEETS D; PERDON L; VANBENNEKOM CA; DAHL N; BAKKER E; OOSTRA BA MULTIPOINT LINKAGE ANALYSIS OF DXS369 AND DXS304 IN FRAGILE-X FAMILIES | 4 | 7 |
| 2136 | 15 | 21 | 943 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):320-327 VANOOST BA; SMITS APT; DREESEN JCFM; VANDENOUWELAND AMW; OOSTRA BA VALIDATION OF LINKAGE-BASED DNA-DIAGNOSIS OF FRAGILE-X GENE CARRIERS WITH THE CGG REPEAT PROBE | 2 | 4 |
| 2137 | 12 | 38 | 1611 1997 JOURNAL OF MEDICAL GENETICS 34(11):907-911 vanRijn MA; deVries BBA; Tibben A; vandenOuweland AMW; Halley DJJ; Niermeijer MF DNA testing for fragile X syndrome: implications for parents and family | 3 | 4 |
| 2138 | 4 | 12 | 145 1983 JOURNAL OF MEDICAL GENETICS 20(4):286-289 VANROY BC; DESMEDT MC; RAES RA; DUMON JE; LEROY JG FRAGILE X TRAIT IN A LARGE KINDRED - TRANSMISSION ALSO THROUGH NORMAL MALES | 20 | 31 |
| 2139 | 9 | 16 | 679 1990 AMERICAN JOURNAL OF MEDICAL GENETICS 36(1):122-125 VANROY BC; WILLEMS PJ; VITS LJ; CEULEMANS BP; COUCKE PJ; VANDERAUWERA BJ; LORMANS JAG; DUMON JE 2 BROTHERS WITH MENTAL-RETARDATION DISCORDANT FOR THE FRAGILE-X SYNDROME | 3 | 4 |
| 2140 | 6 | 28 | 293 1985 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 6(2):87-90 VARLEY CK; HOLM VA; EREN MO COGNITIVE AND PSYCHIATRIC VARIABILITY IN 3 BROTHERS WITH FRAGILE X-SYNDROME | 10 | 13 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2141 | 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 |
| 2142 | 17 | 31 | 572 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 |
| 2143 | 13 | 33 | 472 1987 JOURNAL OF MEDICAL GENETICS 24(7):413-421 VEENEMA H; CARPENTER NJ; BAKKER E; HOFKER MH; WARD AM; PEARSON PL THE FRAGILE-X SYNDROME IN A LARGE FAMILY .3. INVESTIGATIONS ON LINKAGE OF FLANKING DNA MARKERS WITH THE FRAGILE SITE-XQ27 | 17 | 38 |
| 2144 | 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 |
| 2145 | 17 | 38 | 469 1987 JOURNAL OF MEDICAL GENETICS 24(1):23-31 VEENEMA H; GERAEDTS JPM; BEVERSTOCK GC; PEARSON PL THE FRAGILE X-SYNDROME IN A LARGE FAMILY .1. CYTOGENETIC AND CLINICAL INVESTIGATIONS | 14 | 21 |
| 2146 | 5 | 21 | 470 1987 JOURNAL OF MEDICAL GENETICS 24(1):32-38 VEENEMA H; VEENEMA T; GERAEDTS JPM THE FRAGILE X-SYNDROME IN A LARGE FAMILY .2. PSYCHOLOGICAL INVESTIGATIONS | 28 | 39 |
| 2147 | 5 | 25 | 147 1983 JOURNAL OF MEDICAL GENETICS 20(6):404-407 VEKEMANS M; POPOVICH B; ROSENBLATT D; MONROE P CHROMOSOMAL BREAKAGE IN NORMAL AND FRAGILE-X SUBJECTS USING LOW FOLATE CULTURE CONDITIONS | 12 | 21 |
| 2148 | 40 | 62 | 1480 1996 GIORNALE DI NEUROPSICHIATRIA DELL ETA EVOLUTIVA 16(2):147-154 Veneselli E; Biancheri R; Perrone MV Neuropsychiatric aspects in the fragile X syndrome | 0 | 0 |
| 2149 | 3 | 6 | 232 1984 PRENATAL DIAGNOSIS 4(6):473-474 VENTER PA; COETZEE DJ; BADENHORST A; MARX MP; HOF JO; BEHARI D; WILMOT J; BATTSON SA A CONFIRMED PRENATAL-DIAGNOSIS OF A FEMALE FETUS WITH THE FRAGILE X-CHROMOSOME | 1 | 4 |
| 2150 | 0 | 0 | 1717 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A471-A471 Ventura KA; Fraer LM; Smith EE; Merrill AE; Treat KJ; Wang Z; Allitto BA; DeMarchi JM; Hogge WA Transmission on a fragile X full mutation through a normal transmitting male. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2151 | 8 | 17 | 1132 1993 NATURE 363(6431):722-724 VERHEIJ C; BAKKER CE; DEGRAAFF E; KEULEMANS J; WILLEMSEN R; VERKERK AJMH; GALJAARD H; REUSER AJJ; HOOGEVEEN AT; OOSTRA BA CHARACTERIZATION AND LOCALIZATION OF THE FMR-1 GENE-PRODUCT ASSOCIATED WITH FRAGILE-X SYNDROME | 103 | 182 |
| 2152 | 8 | 24 | 1098 1993 HUMAN MOLECULAR GENETICS 2(4):399-404 VERKERK AJMH; DEGRAAFF E; DEBOULLE K; EICHLER EE; KONECKI DS; REYNIERS E; MANCA A; POUSTKA A; WILLEMS PJ; NELSON DL; OOSTRA BA ALTERNATIVE SPLICING IN THE FRAGILE X-GENE FMR1 | 0 | 75 |
| 2153 | 0 | 1 | 1099 1993 HUMAN MOLECULAR GENETICS 2(8):1348-1348 VERKERK AJMH; DEGRAAFF E; DEBOULLE K; EICHLER EE; KONECKI DS; REYNIERS E; MANCA A; POUSTKA A; WILLEMS PJ; NELSON DL; OOSTRA BA ALTERNATIVE SPLICING IN THE FRAGILE X-GENE FMR1 (VOL 2, PG 399, 1993) | 3 | 6 |
| 2154 | 9 | 13 | 931 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):192-196 VERKERK AJMH; DEVRIES BBA; NIERMEIJER MF; FU YH; NELSON DL; WARREN ST; MAJOORKRAKAUER DF; HALLEY DJJ; OOSTRA BA INTRAGENIC PROBE USED FOR DIAGNOSTICS IN FRAGILE-X FAMILIES | 5 | 6 |
| 2155 | 10 | 17 | 930 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):187-191 VERKERK AJMH; EUSSEN BHJ; VANHEMEL JO; OOSTRA BA LIMITED SIZE OF THE FRAGILE-X SITE SHOWN BY FLUORESCENCE INSITU HYBRIDIZATION | 6 | 7 |
| 2156 | 11 | 40 | 839 1991 CELL 65(5):905-914 VERKERK AJMH; PIERETTI M; SUTCLIFFE JS; FU YH; KUHL DPA; PIZZUTI A; REINER O; RICHARDS S; VICTORIA MF; ZHANG FP; EUSSEN BE; VANOMMEN GJB; BLONDEN LAJ; RIGGINS GJ; CHASTAIN JL; KUNST CB; GALJAARD H; CASKEY CT; NELSON DL; OOSTRA BA; WARREN ST IDENTIFICATION OF A GENE (FMR-1) CONTAINING A CGG REPEAT COINCIDENT WITH A BREAKPOINT CLUSTER REGION EXHIBITING LENGTH VARIATION IN FRAGILE-X SYNDROME | 501 | 1246 |
| 2157 | 1 | 2 | 483 1987 LANCET 2(8554):329-329 VERLOES A; SACRE JP; GEUBELLE F SOTOS SYNDROME AND FRAGILE-X CHROMOSOMES | 1 | 5 |
| 2158 | 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 |
| 2159 | 4 | 6 | 1737 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):326-326 Vianna-Morgante AM Twinning and premature ovarian failure in premutation fragile X carriers | 8 | 9 |
| 2160 | 6 | 8 | 1829 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(1):254-255 Vianna-Morgante AM; Costa SS Premature ovarian failure is associated with maternally and paternally inherited premutation in Brazilian families with fragile X | 8 | 15 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2161 | 5 | 14 | 1788 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 |
| 2162 | 5 | 5 | 946 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 |
| 2163 | 4 | 44 | 566 1988 BRAIN AND LANGUAGE 34(2):203-221 VILKMAN E; NIEMI J; IKONEN U FRAGILE-X SPEECH PHONOLOGY IN FINNISH | 4 | 5 |
| 2164 | 0 | 0 | 640 1989 GENOMICS 5(4):797-801 VINCENT A; DAHL N; OBERLE I; HANAUER A; MANDEL JL; MALMGREN H; PETTERSSON U THE POLYMORPHIC MARKER DXS304 IS WITHIN 5-CENTIMORGANS OF THE FRAGILE-X LOCUS | 13 | 23 |
| 2165 | 11 | 14 | 882 1991 NATURE 349(6310):624-626 VINCENT A; HEITZ D; PETIT C; KRETZ C; OBERLE I; MANDEL JL ABNORMAL PATTERN DETECTED IN FRAGILE-X PATIENTS BY PULSED-FIELD GEL-ELECTROPHORESIS | 105 | 164 |
| 2166 | 2 | 4 | 1665 1998 HUMAN MUTATION 12(6):431-431 Vincent JB; Gurling HMD Point mutation in intron 10 of FMR1 is unlikely to be a cause of fragile X syndrome | 3 | 5 |
| 2167 | 6 | 7 | 2095 2002 AMERICAN JOURNAL OF MEDICAL GENETICS 107(4):344-345 Vink GR; Froster UG Comparison of FMR1-protein expression in lymphocytes, methylation pattern in Southern blot analysis, and IQ values in three sisters with the fragile X syndrome | 0 | 1 |
| 2168 | 16 | 24 | 590 1988 HUMAN GENETICS 80(4):375-378 VOELCKEL MA; MATTEI MG; NGUYEN C; PHILIP N; BIRG F; MATTEI JF DISSOCIATION BETWEEN MENTAL-RETARDATION AND FRAGILE SITE EXPRESSION IN A FAMILY WITH FRAGILE X-LINKED MENTAL-RETARDATION | 8 | 16 |
| 2169 | 13 | 25 | 801 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):374-377 VOELCKEL MA; PELLISSIER MC; PIQUET C; NGUYEN C; BOCCACCIO I; PHILIP N; MATTEI JF FRAGILE-X SYNDROME IN AN EXTENDED FAMILY WITH SPECIAL REFERENCE TO AN AFFECTED MALE WITH KLINEFELTER SYNDROME | 2 | 2 |
| 2170 | 4 | 53 | 2149 2002 JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY AND ALLIED DISCIPLINES 43(7):949-957 von Gontard A; Backes M; Laufersweiler-Plass C; Wendland C; Lehmkuhl G; Zerres K; Rudnik-Schoneborn S Psychopathology and familial stress - comparison of boys with Fragile X syndrome and Spinal Muscular Atrophy | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2171 | 0 | 0 | 1635 1998 AMERICAN JOURNAL OF MEDICAL GENETICS 81(6):552-552 von Gontard A; Backes M; Schreck J; Genc B; Doerfler W Behavioural phenotype of the fragile-X-syndrome. | 0 | 0 |
| 2172 | 29 | 39 | 666 1989 ZEITSCHRIFT FUR KINDER-UND JUGENDPSYCHIATRIE UND PSYCHOTHERAPIE 17(2):91-97 VONGONTARD A PSYCHOPATHOLOGY ASSOCIATED WITH THE FRAGILE-X SYNDROME | 1 | 2 |
| 2173 | 19 | 26 | 1018 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 |
| 2174 | 13 | 28 | 284 1985 HUMAN GENETICS 69(3):218-223 VONKOSKULL H; AULA P; AMMALA P; NORDSTROM AM; RAPOLA J IMPROVED TECHNIQUE FOR THE EXPRESSION OF FRAGILE-X IN CULTURED AMNIOTIC-FLUID CELLS | 5 | 9 |
| 2175 | 8 | 10 | 1185 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):486-489 VONKOSKULL H; GAHMBERG N; SALONEN R; SALO A; PEIPPO M FRAXA LOCUS IN FRAGILE-X DIAGNOSIS - FAMILY STUDIES, PRENATAL-DIAGNOSIS, AND DIAGNOSIS OF SPORADIC CASES OF MENTAL-RETARDATION | 8 | 8 |
| 2176 | 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 |
| 2177 | 71 | 144 | 1701 1998 ZHURNAL NEVROPATOLOGII I PSIKHIATRII IMENI S S KORSAKOVA 98(9):54-63 Vorsanova SG; Vekhova NV; Demidova IA; Yurov YB Syndrome of mental retardation, linked with fragile X-chromosome: problems of diagnostics and inheritance | 0 | 0 |
| 2178 | 1 | 8 | 1074 1993 BRITISH JOURNAL OF HAEMATOLOGY 85(2):415-416 VORST EJ; LEVENE NA; NISANI R; BERREBI A FRAGILE-X SYNDROME AND MYELODYSPLASIA DISCOVERED DURING PREGNANCY | 3 | 5 |
| 2179 | 4 | 9 | 648 1989 JOURNAL OF MEDICAL GENETICS 26(7):439-442 VOULLAIRE LE; WEBB GC; LEVERSHA M FRAGILE X-TESTING IN A DIAGNOSTIC CYTOGENETICS LABORATORY | 3 | 7 |
| 2180 | 0 | 0 | 1636 1998 AMERICAN JOURNAL OF PATHOLOGY 153(5):1651-1651 Wages J; Bloch W; Burman R; Popovich B; Kruckeberg KE; Tester DJ; Snow K Size accuracy in a fragile X size-polymorphism assay | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2181 | 6 | 18 | 337 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):403-408 WAHLSTROM J; GILLBERG C; GUSTAVSON KH; HOLMGREN G INFANTILE-AUTISM AND THE FRAGILE-X - A SWEDISH MULTICENTER STUDY | 23 | 44 |
| 2182 | 0 | 1 | 638 1989 CYTOGENETICS AND CELL GENETICS 51(1-4):1100-1101 WAHLSTROM J; WITTENGERSTROM I; ANVRET M; ODEN A; JOHANNESSON T; HOLMQUIST D RETT SYNDROME RELATED TO FRAGILE X(P22) IN CAFFEINE-INDUCED LYMPHOCYTES CULTURES | 0 | 2 |
| 2183 | 1 | 14 | 691 1990 BRAIN & DEVELOPMENT 12(1):128-130 WAHLSTROM J; WITTENGERSTROM I; MELLQUIST L; ANVRET M; ODEN A THE RETT SYNDROME RELATED TO FRAGILE-X(P22) IN CAFFEINE-INDUCED LYMPHOCYTE CULTURE | 0 | 13 |
| 2184 | 11 | 21 | 1334 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):319-326 Wake SA; Robinson H Assessment of counselling of normal males and normal transmitting male carriers identified in fragile X families | 0 | 0 |
| 2185 | 0 | 0 | 2039 2001 JOURNAL OF MEDICAL GENETICS 38:S64-S64 Wakeling W; King W; Taylor R Chemiluminescence detection offers a safe, effective and convenient alternative to radioisotopic labelling of probes for detection of Fragile X syndrome and other single gene disorders | 0 | 0 |
| 2186 | 24 | 41 | 2304 2003 PRENATAL DIAGNOSIS 23(4):345-351 Wald NJ; Morris JK A new approach to antenatal screening for Fragile X syndrome | 1 | 1 |
| 2187 | 0 | 1 | 2366 2004 PRENATAL DIAGNOSIS 24(1):68-69 Wald NJ; Morris JK Reply: Prenatal screen for Fragile X syndrome | 0 | 0 |
| 2188 | 8 | 20 | 511 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):83-98 WALDSTEIN G; HAGERMAN R AORTIC HYPOPLASIA AND CARDIAC VALVULAR ABNORMALITIES IN A BOY WITH FRAGILE-X SYNDROME | 5 | 5 |
| 2189 | 30 | 74 | 1946 2000 MOLECULAR AND CELLULAR BIOLOGY 20(22):8536-8547 Wan LL; Dockendorff TC; Jongens TA; Dreyfuss G Characterization of dFMR1, a Drosophila melanogaster homolog of the fragile X mental retardation protein | 33 | 42 |
| 2190 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2191 | 0 | 1 | 46 1982 AMERICAN JOURNAL OF HUMAN GENETICS 34(6):A149-A149 WANG JC; BOSS GR; MAGNER MT; ERBE RW FOLATE PATHWAYS IN CELLS FROM FRAGILE-X SYNDROME PATIENTS AND CARRIERS | 2 | 3 |
| 2192 | 1 | 12 | 245 1985 AMERICAN JOURNAL OF MEDICAL GENETICS 21(4):691-696 WANG JCC; BEARDSLEY GP; ERBE RW ANTIFOLATE-INDUCED MISINCORPORATION OF DEOXYURIDINE MONOPHOSPHATE INTO DNA BY CELLS FROM PATIENTS WITH THE FRAGILE-X SYNDROME | 2 | 5 |
| 2193 | 2 | 11 | 184 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):303-310 WANG JCC; ERBE RW FOLATE METABOLISM IN CELLS FROM FRAGILE-X SYNDROME PATIENTS AND CARRIERS | 15 | 22 |
| 2194 | 4 | 15 | 310 1985 SOMATIC CELL AND MOLECULAR GENETICS 11(4):353-357 WANG JCC; ERBE RW THYMIDYLATE METABOLISM IN FRAGILE-X SYNDROME CELLS | 3 | 5 |
| 2195 | 6 | 9 | 1127 1993 LANCET 342(8878):1025-1026 WANG Q; GREEN E; BARNICOAT A; GARRETT D; MULLARKEY M; BOBROW M; MATHEW CG CYTOGENETIC VERSUS DNA DIAGNOSIS IN ROUTINE REFERRALS FOR FRAGILE-X SYNDROME | 15 | 22 |
| 2196 | 10 | 20 | 1371 1995 JOURNAL OF MEDICAL GENETICS 32(3):170-173 WANG Q; GREEN E; BOBROW M; MATHEW CG A RAPID, NONRADIOACTIVE SCREENING-TEST FOR FRAGILE-X MUTATIONS AT THE FRAXA AND FRAXE LOCI | 15 | 27 |
| 2197 | 0 | 0 | 1368 1995 JOURNAL OF MEDICAL GENETICS 32(2):153-153 WANG Q; GREEN EP; BOBROW M; MATHEW CG SCREENING FOR THE FRAGILE-X A-MUTATION AND E-MUTATION BY AUTOMATED FLUORESCENT ANALYSIS | 0 | 0 |
| 2198 | 0 | 0 | 1237 1994 JOURNAL OF MEDICAL GENETICS 31(2):173-173 WANG Q; GREEN EP; MATHEW CG; BOBROW M NONRADIOACTIVE PCR BASED SCREENING FOR FRAGILE-X SYNDROME | 0 | 0 |
| 2199 | 11 | 35 | 2107 2002 ARCHIVES OF MEDICAL RESEARCH 33(2):128-135 Wang TS; Hsieh LJ; Hsu TY; Chung CH; Li SY DNA damage and repair in lymphoblastoid cell lines from normal donors and fragile X syndrome patients | 0 | 1 |
| 2200 | 11 | 17 | 1942 2000 JOURNAL OF THE FORMOSAN MEDICAL ASSOCIATION 99(5):402-407 Wang YC; Li C; Lin ML; Lin WH; Li SY Molecular diagnosis of fragile X syndrome and distribution of CGG repeats in the FMR-1 gene in Taiwanese | 0 | 0 |
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