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Nodes: 2369
Authors: 4634,
Journals: 373,
Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by journal name.
Page 12: 1 (A N A E-APPROCHE NEUROPSYCHOLOGIQUE DES APPRENTISSAGES CHEZ L ENFANT) 2 (AMERICAN JOURNAL OF HUMAN GENETICS) 3 (AMERICAN JOURNAL OF HUMAN GENETICS) 4 (AMERICAN JOURNAL OF HUMAN GENETICS) 5 (AMERICAN JOURNAL OF MEDICAL GENETICS) 6 (AMERICAN JOURNAL OF MEDICAL GENETICS) 7 (AMERICAN JOURNAL OF MEDICAL GENETICS) 8 (AMERICAN JOURNAL OF MEDICAL GENETICS) 9 (AMERICAN JOURNAL OF MEDICAL GENETICS) 10 (ANNALS OF NEUROLOGY) 11 (BIOPHYSICAL JOURNAL) 12 (CLINICAL GENETICS) 13 (CURRENT BIOLOGY) 14 (DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY) 15 (GENETIC TESTING) 16 (HUMAN GENETICS) 17 (JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION) 18 (JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS) 19 (JOURNAL OF MEDICAL GENETICS) 20 (JOURNAL OF NEUROSCIENCE RESEARCH) 21 (MEDICAL ANTHROPOLOGY QUARTERLY) 22 (NATURE REVIEWS NEUROSCIENCE) 23 (PEDIATRIC RESEARCH) 24 (REVISTA DE NEUROLOGIA)
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 1101 | 8 | 23 | 126 1983 CLINICAL GENETICS 23(6):436-440 SILVERMAN W; LUBIN R; JENKINS EC; BROWN WT THE STRENGTH OF ASSOCIATION BETWEEN FRAGILE(X) CHROMOSOME PRESENCE AND MENTAL-RETARDATION | 8 | 11 |
| 1102 | 3 | 11 | 127 1983 CLINICAL GENETICS 24(3):153-155 NIELSEN KB; TOMMERUP N; FRIIS B; HJELT K; HIPPE E FOLIC-ACID METABOLISM IN A PATIENT WITH FRAGILE-X | 0 | 9 |
| 1103 | 1 | 4 | 128 1983 CLINICAL GENETICS 24(5):320-323 DEARCE MA TABLES FOR THE CYTOGENETIC STUDY OF FRAGILE X-CHROMOSOMES FOR DIAGNOSTIC PURPOSES | 11 | 17 |
| 1104 | 3 | 15 | 129 1983 CLINICAL GENETICS 24(6):393-398 BLOMQUIST HK; GUSTAVSON KH; HOLMGREN G; NORDENSON I; PALSSONSTRAE U FRAGILE X-SYNDROME IN MILDLY MENTALLY-RETARDED CHILDREN IN A NORTHERN SWEDISH COUNTY - A PREVALENCE STUDY | 42 | 67 |
| 1105 | 0 | 3 | 191 1984 CLINICAL GENETICS 25(2):131-134 FRYNS JP; JACOBS J; KLECZKOWSKA A; VANDENBERGHE H THE PSYCHOLOGICAL PROFILE OF THE FRAGILE X-SYNDROME | 56 | 75 |
| 1106 | 1 | 9 | 192 1984 CLINICAL GENETICS 25(2):135-139 GARDINER GB; WENGER SL; STEELE MW INVITRO REVERSAL OF FRAGILE-X EXPRESSION BY EXOGENOUS THYMIDINE | 5 | 7 |
| 1107 | 2 | 11 | 193 1984 CLINICAL GENETICS 26(5):445-447 FRYNS JP; KLECZKOWSKA A; WOLFS I; VANDENBERGHE H KLINEFELTER SYNDROME AND 2 FRAGILE X-CHROMOSOMES | 15 | 21 |
| 1108 | 21 | 64 | 194 1984 CLINICAL GENETICS 26(6):497-528 FRYNS JP THE FRAGILE X-SYNDROME - A STUDY OF 83 FAMILIES | 45 | 78 |
| 1109 | 7 | 27 | 259 1985 CLINICAL GENETICS 27(2):113-117 BLOMQUIST HK; BOHMAN M; EDVINSSON SO; GILLBERG C; GUSTAVSON KH; HOLMGREN G; WAHLSTROM J FREQUENCY OF THE FRAGILE X-SYNDROME IN INFANTILE-AUTISM - A SWEDISH MULTICENTER STUDY | 50 | 84 |
| 1110 | 2 | 8 | 260 1985 CLINICAL GENETICS 27(2):118-121 HIRTH L; SINGH S; SCHILLING S; MULLER E; GOEDDE HW DERMATOGLYPHIC FINDINGS IN PATIENTS WITH FRAGILE X-CHROMOSOME | 2 | 6 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1111 | 0 | 0 | 261 1985 CLINICAL GENETICS 27(3):307-307 FRYNS JP THE FRAGILE-X SYNDROME - A STUDY OF 83 INDEX-PATIENTS AND THEIR FAMILIES | 0 | 1 |
| 1112 | 0 | 0 | 262 1985 CLINICAL GENETICS 27(3):334-335 SCHMIDT A PRENATAL-DIAGNOSIS OF FRAGILE X-SYNDROME | 2 | 4 |
| 1113 | 6 | 18 | 263 1985 CLINICAL GENETICS 27(5):463-467 GUSTAVSON KH; DAHLBOM K; FLOOD A; HOLMGREN G; BLOMQUIST HK; SANNER G EFFECT OF FOLIC-ACID TREATMENT IN THE FRAGILE X-SYNDROME | 10 | 14 |
| 1114 | 4 | 8 | 264 1985 CLINICAL GENETICS 27(5):520-521 WEBB GC DETECTION OF THE FRAGILE X-CHROMOSOME AND OTHER FRAGILE SITES | 5 | 6 |
| 1115 | 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 |
| 1116 | 4 | 11 | 266 1985 CLINICAL GENETICS 28(2):97-99 ABUELO D; CASTREE K; PUESCHEL S; PADREMENDOZA T; ZOLNIERZ K FREQUENCY OF FRAGILE X-CHROMOSOME IN NORMAL FEMALES | 2 | 5 |
| 1117 | 3 | 6 | 267 1985 CLINICAL GENETICS 28(5):399-400 SOUDEK D DECREASE OF FRAGILE X-FREQUENCY IN STORED-BLOOD SAMPLES - INDIVIDUAL VARIABILITY | 1 | 1 |
| 1118 | 0 | 0 | 268 1985 CLINICAL GENETICS 28(5):422-423 DAVIES KE; OLD J; MCGLADE S; SPEER A; COUTELLE C; PEMBREY M; HARPER K LINKAGE OF RFLPS AROUND THE DMD AND BMD LOCI AND THE FRAGILE X-LOCUS | 0 | 0 |
| 1119 | 0 | 0 | 269 1985 CLINICAL GENETICS 28(5):449-449 MAVROU A; SYRROU M; TSENGHI C; AGELAKIS M; YOUROUKOS S; METAXOTOU C FRAGILE X-SYNDROME AND MENTAL-RETARDATION IN GREECE | 0 | 0 |
| 1120 | 3 | 5 | 373 1986 CLINICAL GENETICS 29(2):95-95 DEARCE MA; HECHT F; SUTHERLAND GR; WEBB GC GUIDELINES FOR THE DIAGNOSIS OF FRAGILE X | 0 | 2 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1121 | 2 | 7 | 374 1986 CLINICAL GENETICS 29(3):191-195 HECHT F; FRYNS JP; VLIETINCK RF; VANDENBERGHE H GENETIC-CONTROL OVER FRAGILE X-CHROMOSOME EXPRESSION | 9 | 10 |
| 1122 | 0 | 0 | 375 1986 CLINICAL GENETICS 29(5):462-462 GOONEWARDENA P; GUSTAVSON KH; HOLMGREN G; TOLUN A; CHOTAI J; JOHNSEN E; PETTERSSON U STUDIES ON FRAGILE X-MENTAL RETARDATION BY THE USE OF DNA PROBES | 1 | 1 |
| 1123 | 2 | 4 | 376 1986 CLINICAL GENETICS 29(5):475-475 TOMMERUP N THE FRAGILE X-CHROMOSOME - PRENATAL-DIAGNOSIS | 1 | 3 |
| 1124 | 7 | 12 | 377 1986 CLINICAL GENETICS 30(4):249-254 GOONEWARDENA P; GUSTAVSON KH; HOLMGREN G; TOLUN A; CHOTAI J; JOHNSEN E; PETTERSSON U ANALYSIS OF FRAGILE X-MENTAL RETARDATION FAMILIES USING FLANKING POLYMORPHIC DNA PROBES | 7 | 13 |
| 1125 | 4 | 5 | 378 1986 CLINICAL GENETICS 30(4):346-347 SOUDEK D FRAGILE-X - EXPERIENCE OF A LABORATORY | 3 | 3 |
| 1126 | 9 | 37 | 434 1987 CLINICAL GENETICS 32(3):179-186 BORGHGRAEF M; FRYNS JP; DIELKENS A; PYCK K; VANDENBERGHE H FRAGILE (X) SYNDROME - A STUDY OF THE PSYCHOLOGICAL PROFILE IN 23 PREPUBERTAL PATIENTS | 46 | 56 |
| 1127 | 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 |
| 1128 | 1 | 13 | 571 1988 CLINICAL GENETICS 33(5):349-355 MERYASH DL; ABUELO D COUNSELING NEEDS AND ATTITUDES TOWARD PRENATAL-DIAGNOSIS AND ABORTION IN FRAGILE-X FAMILIES | 5 | 17 |
| 1129 | 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 |
| 1130 | 0 | 0 | 573 1988 CLINICAL GENETICS 33(6):464-464 HULTEN M; JOHANNISSON R MEIOSIS IN THE FRAGILE-X MENTAL-RETARDATION SYNDROME | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1131 | 7 | 21 | 574 1988 CLINICAL GENETICS 34(4):265-271 ANVRET M; GILLBERG C; WAHLSTROM J; ALBERTSSONWIKLAND K; DAVIES K INFANTILE-AUTISM, FRAGILE (X) (Q27.3) AND RFLP ANALYSIS IN AN EXTENDED SWEDISH FAMILY | 2 | 4 |
| 1132 | 2 | 31 | 629 1989 CLINICAL GENETICS 36(1):15-24 MERYASH DL PERCEPTION OF BURDEN AMONG AT-RISK WOMEN OF RAISING A CHILD WITH FRAGILE-X SYNDROME | 2 | 7 |
| 1133 | 9 | 14 | 630 1989 CLINICAL GENETICS 36(1):25-30 TUCKERMAN E; WEBB T THE INACTIVATION OF THE FRAGILE X-CHROMOSOME IN FEMALE CARRIERS OF THE MARTIN-BELL SYNDROME AS STUDIED BY 2 DIFFERENT METHODS | 4 | 6 |
| 1134 | 24 | 44 | 694 1990 CLINICAL GENETICS 37(1):2-11 SUTHERLAND GR; MULLEY JC DIAGNOSTIC MOLECULAR-GENETICS OF THE FRAGILE-X | 14 | 16 |
| 1135 | 5 | 23 | 695 1990 CLINICAL GENETICS 37(3):167-172 SUTHERLAND GR; BAKER E THE COMMON FRAGILE SITE IN BAND Q27 OF THE HUMAN X-CHROMOSOME IS NOT COINCIDENT WITH THE FRAGILE-X | 29 | 43 |
| 1136 | 13 | 27 | 696 1990 CLINICAL GENETICS 37(5):341-346 BORGHGRAEF M; FRYNS JP; VANDENBERGHE H THE FEMALE AND THE FRAGILE X-SYNDROME - DATA ON CLINICAL AND PSYCHOLOGICAL FINDINGS IN 7 FRA(X) CARRIERS | 16 | 20 |
| 1137 | 5 | 10 | 842 1991 CLINICAL GENETICS 39(5):347-354 BUTLER MG; MANGRUM T; GUPTA R; SINGH DN A 15-ITEM CHECKLIST FOR SCREENING MENTALLY-RETARDED MALES FOR THE FRAGILE X-SYNDROME | 28 | 32 |
| 1138 | 15 | 22 | 968 1992 CLINICAL GENETICS 42(1):22-26 MARTINEZ F; BADIA L; PRIETO F A FRAGILE-X FAMILY WITH HIGH PENETRANCE IN FEMALES - RISK HETEROGENEITY | 0 | 2 |
| 1139 | 20 | 26 | 1077 1993 CLINICAL GENETICS 43(1):34-38 HORI T; YAMAUCHI M; SEKI N; TSUJI S; IKUKO K HERITABLE UNSTABLE DNA-SEQUENCES AND HYPERMETHYLATION ASSOCIATED WITH FRAGILE-X SYNDROME IN JAPANESE FAMILIES | 9 | 13 |
| 1140 | 7 | 7 | 1078 1993 CLINICAL GENETICS 43(3):157-159 MORNET E; JOKIC M; BOGYO A; TEJADA I; DELUCHAT C; BOUE J; BOUE A AFFECTED SIBS WITH FRAGILE-X SYNDROME EXHIBIT AN AGE-DEPENDENT DECREASE IN THE SIZE OF THE FRAGILE-X FULL MUTATION | 5 | 8 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1141 | 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 |
| 1142 | 7 | 11 | 1080 1993 CLINICAL GENETICS 44(2):109-110 BODURTHA J; JACKSONCOOK C; MADDALENA A; PISERCHIO J; WALLER R 46XY/47XYY MOSAICISM AND FRAGILE-X | 3 | 4 |
| 1143 | 18 | 37 | 1081 1993 CLINICAL GENETICS 44(3):129-138 BUTLER MG; PRATESI R; WATSON MS; BREG WR; SINGH DN ANTHROPOMETRIC AND CRANIOFACIAL PATTERNS IN MENTALLY-RETARDED MALES WITH EMPHASIS ON THE FRAGILE-X SYNDROME | 4 | 8 |
| 1144 | 16 | 20 | 1082 1993 CLINICAL GENETICS 44(4):169-172 YAMAUCHI M; NAGATA S; SEKI N; TOYAMA Y; HARADA N; NIIKAWA N; MASUNO I; KAJII T; HORI T PRENATAL-DIAGNOSIS OF FRAGILE X-SYNDROME BY DIRECT-DETECTION OF THE DYNAMIC MUTATION DUE TO AN UNSTABLE DNA-SEQUENCE | 2 | 5 |
| 1145 | 10 | 23 | 1209 1994 CLINICAL GENETICS 45(4):175-180 SCHRANDERSTUMPEL C; GERVER WJ; MEYER H; ENGELEN J; MULDER H; FRYNS JP PRADER-WILLI-LIKE PHENOTYPE IN FRAGILE-X SYNDROME | 4 | 17 |
| 1146 | 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 |
| 1147 | 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 |
| 1148 | 1 | 9 | 1576 1997 CLINICAL GENETICS 51(1):71-74 Behjati F; Mullarkey M; Bergbaum A; Berry AC; Docherty Z Chromosome deletion 17p11.2 (Smith-Magenis syndrome) in seven new patients, four of whom had been referred for fragile-X investigation | 0 | 5 |
| 1149 | 9 | 15 | 1577 1997 CLINICAL GENETICS 52(3):147-154 Hecimovic S; Barisic I; Muller A; Petkovic I; Baric I; Ligutic I; Pavelic K Expand long PCR for fragile X mutation detection | 8 | 23 |
| 1150 | 11 | 14 | 1578 1997 CLINICAL GENETICS 52(4):211-215 Arvio M; Peippo M; Simola KOJ Applicability of a checklist for clinical screening of the fragile X syndrome | 10 | 13 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1151 | 12 | 28 | 1642 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 |
| 1152 | 8 | 10 | 1643 1998 CLINICAL GENETICS 53(3):200-201 Mornet E; Chateau C; Simon-Bouy B; Serre JL The intermediate alleles of the fragile X CGG repeat in patients with mental retardation | 3 | 6 |
| 1153 | 18 | 30 | 1644 1998 CLINICAL GENETICS 54(4):309-314 Russo S; Briscioli V; Cogliati F; Macchi M; Lalatta F; Larizza L An unusual fragile X sibship: female compound heterozygote and male with a partially methylated full mutation | 0 | 1 |
| 1154 | 0 | 2 | 1645 1998 CLINICAL GENETICS 54(4):365-365 Toro-Sola MA Fragile X and Rett syndromes in Puerto Rico | 0 | 0 |
| 1155 | 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 |
| 1156 | 34 | 44 | 1773 1999 CLINICAL GENETICS 55(5):346-351 Tassone F; Longshore J; Zunich J; Steinbach P; Salat U; Taylor AK Tissue-specific methylation differences in a fragile X premutation carrier | 2 | 4 |
| 1157 | 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 |
| 1158 | 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 |
| 1159 | 20 | 33 | 1881 2000 CLINICAL GENETICS 58(2):111-115 Kallinen J; Heinonen S; Mannermaa A; Ryynanen M Prenatal diagnosis of fragile X syndrome and the risk of expansion of a premutation | 3 | 5 |
| 1160 | 52 | 100 | 2009 2001 CLINICAL GENETICS 60(6):399-408 Oostra BA; Chiurazzi P The fragile X gene and its function | 5 | 9 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1161 | 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 |
| 1162 | 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 |
| 1163 | 0 | 1 | 2255 2003 CLINICAL GENETICS 64(2):106-108 Leavitt BR Something lost in the translation: 'premutations' in the FMR1 gene cause Fragile X tremor/ataxia syndrome (FXTAS) | 0 | 0 |
| 1164 | 11 | 21 | 1468 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 |
| 1165 | 4 | 13 | 843 1991 CLINICAL PEDIATRICS 30(5):318-321 HO HH; EAVES LC; PAYNE E VARIABILITY OF DEVELOPMENT IN 3 SIBLINGS WITH FRAGILE-X SYNDROME | 0 | 1 |
| 1166 | 0 | 0 | 17 1981 CLINICAL RESEARCH 29(1):A134-A134 HERBST DS; GERRARD JW; DUNN HG; DILL FJ; KALOUSEK DK; KRYWANIUK LW; KNOLL J; CHUDLEY AE NONSPECIFIC X-LINKED MENTAL-RETARDATION, MACRO-ORCHIDISM AND THE FRAGILE X-CHROMOSOME MARKER | 0 | 0 |
| 1167 | 0 | 0 | 53 1982 CLINICAL RESEARCH 30(2):A291-A291 BROWN WT; JENKINS EC; FRIEDMAN E; WISNIEWSKI K; FRENCH JH THE FRAGILE X-SYNDROME - A GENETIC CAUSE OF AUTISM | 0 | 0 |
| 1168 | 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 |
| 1169 | 0 | 0 | 55 1982 CLINICAL RESEARCH 30(5):A890-A890 KRUMDIECK CL; HOWARDPEEBLES PN THE ORIGIN OF THE FRAGILE X IN HUMAN-CHROMOSOMES - AN HYPOTHESIS | 0 | 0 |
| 1170 | 0 | 0 | 56 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1171 | 0 | 1 | 130 1983 CLINICAL RESEARCH 31(2):A290-A290 BROWN T; JENKINS E; FRIEDMAN E; BROOKS J; DUNCAN C; COHEN I; HILL L; WISNIEWSKI K; FRENCH J FOLIC-ACID THERAPY OF FRAGILE-X SYNDROME | 0 | 0 |
| 1172 | 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 |
| 1173 | 0 | 1 | 132 1983 CLINICAL RESEARCH 31(5):A897-A897 HOWARDPEEBLES PN NORMAL-MALE TRANSMISSION OF THE FRAGILE-X - THE COUNSELING DILEMMA | 0 | 0 |
| 1174 | 0 | 0 | 195 1984 CLINICAL RESEARCH 32(5):A884-A884 FRIEDMAN JM; HOWARDPEEBLES PN A THEORETICAL-MODEL FOR UNAFFECTED CARRIER MALES IN FRAGILE-X FAMILIES | 0 | 0 |
| 1175 | 0 | 0 | 196 1984 CLINICAL RESEARCH 32(5):A885-A885 HOLMAN GH; ALLEN SM; TUCKER DA; TAWATER BA SEIZURES AND UNUSUAL VISUAL EVOKED-RESPONSES IN FRAGILE-X CARRIERS | 0 | 0 |
| 1176 | 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 |
| 1177 | 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 |
| 1178 | 0 | 0 | 435 1987 CLINICAL RESEARCH 35(1):A60-A60 EDWARDS DR; KEPPEN LD; GOLLIN SM AUTISM AND FRAGILE-X SYNDROME | 0 | 0 |
| 1179 | 0 | 0 | 436 1987 CLINICAL RESEARCH 35(1):A60-A60 MIXON JC; DEV VG DIMETHYLSULFOXIDE (DMSO) INCREASES FRAGILE-X (FRA-X) EXPRESSION IN THE PRESENCE OF 5-FLOURO-2'-DEOXYURIDINE (FDUMP) | 0 | 0 |
| 1180 | 0 | 0 | 437 1987 CLINICAL RESEARCH 35(1):A211-A211 HAGERMAN RJ; JACKSON AW; BERRY R; CAMPBELL J; STILLMAN E; SMITH ACM; MCGAVRAN L PREDICTORS OF THE FRAGILE-X SYNDROME | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1181 | 0 | 0 | 575 1988 CLINICAL RESEARCH 36(1):A207-A207 BIXENMAN H; HECHT F; LOCKWOOD D; HECHT BK NEW COMMON FRAGILE SITE AT XQ27.3 CONFOUNDED WITH FRAGILE-X | 0 | 0 |
| 1182 | 0 | 0 | 631 1989 CLINICAL RESEARCH 37(1):A170-A170 HAGERMAN RJ; SCHREINER RA; KEMPER MB; WITTENBERGER MD; ZAHN B; HABICHT K LONGITUDINAL IQ CHANGES IN FRAGILE-X MALES | 0 | 0 |
| 1183 | 0 | 0 | 697 1990 CLINICAL RESEARCH 38(1):A164-A164 HAGERMAN R; AMIRI K; CRONISTER A; WITTENBERGER M; SCHREINER R; SOBESKY W FRAGILE-X GIRLS - PHYSICAL AND NEUROCOGNITIVE STATUS AND OUTCOME | 0 | 0 |
| 1184 | 0 | 0 | 844 1991 CLINICAL RESEARCH 39(1):A1-A1 GOLDSON E; HAGERMAN RJ TEMPERAMENT AND THE FRAGILE-X SYNDROME | 2 | 2 |
| 1185 | 0 | 0 | 845 1991 CLINICAL RESEARCH 39(3):A722-A722 BERRYKRAVIS E; HODGES C DEFECTIVE CYCLIC-AMP PRODUCTION IN TISSUES FROM PATIENTS WITH FRAGILE-X SYNDROME | 0 | 0 |
| 1186 | 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 |
| 1187 | 43 | 78 | 1320 1995 CLINICS IN LABORATORY MEDICINE 15(4):859-& Brown WT Perspectives and molecular diagnosis of the fragile X syndrome | 2 | 2 |
| 1188 | 37 | 73 | 2010 2001 COGNITIVE NEUROPSYCHOLOGY 18(1):1-18 Simon JA; Keenan JM; Pennington BF; Taylor AK; Hagerman RJ Discourse processing in women with fragile X syndrome: Evidence for a deficit establishing coherence | 6 | 7 |
| 1189 | 9 | 45 | 381 1986 COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY 51:195-203 MANDEL JL; ARVEILER B; CAMERINO G; HANAUER A; HEILIG R; KOENIG M; OBERLE I GENETIC-MAPPING OF THE HUMAN X-CHROMOSOME - LINKAGE ANALYSIS OF THE Q26-Q28 REGION THAT INCLUDES THE FRAGILE X-LOCUS AND ISOLATION OF EXPRESSED SEQUENCES | 4 | 36 |
| 1190 | 37 | 74 | 1469 1996 COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY 61:679-687 Eberhart DE; Warren ST The molecular basis of fragile X syndrome | 6 | 8 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1191 | 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 |
| 1192 | 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 |
| 1193 | 9 | 25 | 2011 2001 COMBINATORIAL CHEMISTRY & HIGH THROUGHPUT SCREENING 4(3):265-272 Murray J; Cuckle H Cystic fibrosis and fragile X syndrome: The arguments for antenatal screening | 1 | 2 |
| 1194 | 9 | 28 | 846 1991 COMPREHENSIVE PSYCHIATRY 32(1):83-87 TRANEBAERG L; ORUM A MAJOR DEPRESSIVE DISORDER AS A PROMINENT BUT UNDERESTIMATED FEATURE OF FRAGILE-X SYNDROME | 2 | 4 |
| 1195 | 10 | 13 | 970 1992 COMPTES RENDUS DES SEANCES DE LA SOCIETE DE BIOLOGIE ET DE SES FILIALES 186(4):363-370 BELDJORD C; RICHARD L FRAGILE-X SYNDROME - AN HERITABLE UNSTABLE ELEMENT | 0 | 0 |
| 1196 | 0 | 1 | 1471 1996 CONTEMPORARY PSYCHOLOGY 41(5):488-489 McGraw KO Behavior and development in fragile X syndrome - Dykens,EM, Hodapp,RM, Leckman,JF | 0 | 0 |
| 1197 | 15 | 30 | 1775 1999 CORTEX 35(2):263-271 Cornish KM; Munir F; Cross G Spatial cognition in males with Fragile-X syndrome: Evidence for a neuropsychological phenotype | 12 | 14 |
| 1198 | 16 | 34 | 1083 1993 CURRENT BIOLOGY 3(11):783-786 TROTTIER Y; DEVYS D; MANDEL JL FRAGILE-X SYNDROME - AN EXPANDING STORY | 4 | 8 |
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