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Nodes: 2369
Authors: 4634,
Journals: 373,
Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by NCR.
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| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 1201 | 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 |
| 1202 | 10 | 14 | 1856 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 95(2):105-107 Tuncbilek E; Alikasifoglu M; Aktas D; Duman F; Yanik H; Anar B; Oostra B; Willemsen R Screening for the fragile X syndrome among mentally retarded males by hair root analysis | 6 | 6 |
| 1203 | 11 | 14 | 1875 2000 BRITISH JOURNAL OF OBSTETRICS AND GYNAECOLOGY 107(8):969-972 Kallinen J; Korhonen K; Kortelainen S; Heinonen S; Ryynanen M Pregnancy outcome in carriers of fragile X | 0 | 0 |
| 1204 | 6 | 14 | 1953 2000 NEUROBIOLOGY OF LEARNING AND MEMORY 74(1):80-93 Irwin SA; Swain RA; Christmon CA; Chakravarti A; Weiler IJ; Greenough WT Evidence for altered fragile-x mental retardation protein expression in response to behavioral stimulation (vol 73, pg 87, 2000) | 2 | 2 |
| 1205 | 10 | 14 | 2165 2002 MICROSCOPY RESEARCH AND TECHNIQUE 57(3):156-158 Churchill JD; Beckel-Mitchener A; Weiler IJ; Greenough WT Effects of fragile X syndrome and an FMR1 knockout mouse model on forebrain neuronal cell biology | 0 | 0 |
| 1206 | 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 |
| 1207 | 5 | 13 | 66 1982 HUMAN GENETICS 62(3):285-286 SCHMIDT A; PASSARGE E; SEEMANOVA E; MACEK M PRENATAL DETECTION OF A FETUS HEMIZYGOUS FOR THE FRAGILE X-CHROMOSOME | 12 | 18 |
| 1208 | 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 |
| 1209 | 2 | 13 | 104 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):1270-1275 MIXON JC; DEV VG FRAGILE-X EXPRESSION IS DECREASED BY 5-AZACYTIDINE AND S-ADENOSYLHOMOCYSTEINE | 4 | 9 |
| 1210 | 1 | 13 | 114 1983 ANNALES DE GENETIQUE 26(4):251-253 FRYNS JP; KLECZKOWSKA A; KUBIEN E; PETIT P; HASPESLAGH M; LINDEMANS I; VANDENBERGHE H XY XXY MOSAICISM AND FRAGILE X-SYNDROME | 12 | 17 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1211 | 6 | 13 | 182 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):289-297 BROWN WT; JENKINS EC; FRIEDMAN E; BROOKS J; COHEN IL; DUNCAN C; HILL AL; MALIK MN; MORRIS V; WOLF E; WISNIEWSKI K; FRENCH JH FOLIC-ACID THERAPY IN THE FRAGILE-X SYNDROME | 20 | 28 |
| 1212 | 4 | 13 | 187 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 18(3):483-491 DANIEL A; EKBLOM L; PHILLIPS S CONSTITUTIVE FRAGILE SITES 1P31, 3P14, 6Q26, AND 16Q23 AND THEIR USE AS CONTROLS FOR FALSE-NEGATIVE RESULTS WITH THE FRAGILE(X) | 12 | 50 |
| 1213 | 7 | 13 | 248 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 |
| 1214 | 7 | 13 | 338 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):429-443 LEDBETTER DH; AIRHART SD; NUSSBAUM RL SOMATIC-CELL HYBRID STUDIES OF FRAGILE-(X) EXPRESSION IN A CARRIER FEMALE AND TRANSMITTING MALE | 10 | 18 |
| 1215 | 6 | 13 | 395 1986 JOURNAL OF MEDICAL GENETICS 23(5):407-410 TUCKERMAN E; WEBB T; THAKE A REPLICATION STATUS OF FRAGILE X(Q27.3) IN 13 FEMALE HETEROZYGOTES | 12 | 16 |
| 1216 | 5 | 13 | 415 1987 AMERICAN JOURNAL OF MEDICAL GENETICS 26(4):987-990 MULLEY JC; SUTHERLAND GR FRAGILE-X TRANSMISSION AND THE DETERMINATION OF CARRIER PROBABILITIES FOR GENETIC-COUNSELING | 0 | 11 |
| 1217 | 2 | 13 | 537 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):459-471 THODE A; LAING S; PARTINGTON MW; TURNER G IS THERE A FRAGILE(X) NEGATIVE MARTIN-BELL SYNDROME | 2 | 6 |
| 1218 | 5 | 13 | 541 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):567-580 MULLEY J; TURNER G; BAIN S; SUTHERLAND GR LINKAGE BETWEEN THE FRAGILE-X AND F9, DXS52 (ST14), DXS98 (4D-8) AND DXS105 (CX55.7) | 13 | 20 |
| 1219 | 8 | 13 | 554 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 31(4):735-739 MAVROU A; SYRROU M; TSENGHI C; AGELAKIS M; YOUROUKOS S; METAXOTOU C MARTIN-BELL SYNDROME IN GREECE, WITH REPORT OF ANOTHER 47,XXY FRAGILE X PATIENT | 7 | 10 |
| 1220 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1221 | 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 |
| 1222 | 2 | 13 | 579 1988 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 30(5):646-649 CAMMARATA S; ARCHIDIACONO N; ROMEO G; BENASSI G; GUARINO M; DALESSANDRO R PREVALENCE OF MENTAL-RETARDATION RELATED TO FRAGILE X SYNDROME AND OTHER CHROMOSOMAL-ABNORMALITIES IN THE REPUBLIC OF SAN MARINO | 0 | 2 |
| 1223 | 3 | 13 | 600 1988 JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY AND ALLIED DISCIPLINES 29(4):447-451 GILLBERG C; OHLSON VA; WAHLSTROM J; STEFFENBURG S; BLIX K MONOZYGOTIC FEMALE TWINS WITH AUTISM AND THE FRAGILE-X SYNDROME (AFRAX) | 9 | 19 |
| 1224 | 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 |
| 1225 | 6 | 13 | 693 1990 BRITISH JOURNAL OF HOSPITAL MEDICINE 43(1):17-17 BUNDEY S FRAGILE-X SYNDROME | 1 | 1 |
| 1226 | 5 | 13 | 836 1991 BIOLOGICAL PSYCHIATRY 29(3):298-299 MENDLEWICZ J; HIRSCH D BIPOLAR MANIC-DEPRESSIVE ILLNESS AND THE FRAGILE-X SYNDROME | 0 | 1 |
| 1227 | 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 |
| 1228 | 5 | 13 | 899 1991 SCIENCE 252(5013):1711-1714 KREMER EJ; PRITCHARD M; LYNCH M; YU S; HOLMAN K; BAKER E; WARREN ST; SCHLESSINGER D; SUTHERLAND GR; RICHARDS RI MAPPING OF DNA INSTABILITY AT THE FRAGILE-X TO A TRINUCLEOTIDE REPEAT SEQUENCE P(CCG)N | 200 | 575 |
| 1229 | 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 |
| 1230 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1231 | 10 | 13 | 1114 1993 JOURNAL OF MEDICAL GENETICS 30(2):94-96 SMITS APT; DREESEN JCFM; POST JG; SMEETS DFCM; DEDIESMULDERS C; SPAANSVANDERBIJL T; GOVAERTS LCP; WARREN ST; OOSTRA BA; VANOOST BA THE FRAGILE-X SYNDROME - NO EVIDENCE FOR ANY RECENT MUTATIONS | 27 | 34 |
| 1232 | 4 | 13 | 1141 1993 NERVENHEILKUNDE 12(2):84-86 FROSTER UG CLINICAL AND MOLECULAR ASPECTS OF THE FRAGILE-X FORM OF MENTAL-RETARDATION (MARTIN-BELL SYNDROME) | 0 | 0 |
| 1233 | 6 | 13 | 1144 1993 PEDIATRICS 91(4):714-715 CRABBE LS; BENSKY AS; HORNSTEIN L; SCHWARTZ DC CARDIOVASCULAR-ABNORMALITIES IN CHILDREN WITH FRAGILE-X SYNDROME | 5 | 7 |
| 1234 | 7 | 13 | 1160 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):339-345 FISCH GS; NELSON DL; SNOW K; THIBODEAU SN; CHALIFOUX M; HOLDEN JJA RELIABILITY OF DIAGNOSTIC-ASSESSMENT OF NORMAL AND PREMUTATION STATUS IN THE FRAGILE-X-SYNDROME USING DNA TESTING | 8 | 11 |
| 1235 | 11 | 13 | 1182 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):471-473 HALLEY D; VANDENOUWELAND A; DEELEN W; VERMA I; OOSTRA B STRATEGY FOR RELIABLE PRENATAL DETECTION OF NORMAL-MALE CARRIERS OF THE FRAGILE-X-SYNDROME | 3 | 4 |
| 1236 | 11 | 13 | 1187 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):497-500 SMITS A; SMEETS D; HAMEL B; DREESEN J; DEHAAN A; VANOOST B PREDICTION OF MENTAL STATUS IN CARRIERS OF THE FRAGILE-X MUTATION USING CGG REPEAT LENGTH | 13 | 16 |
| 1237 | 11 | 13 | 1188 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):501-502 KAPLAN G; KUNG M; MCCLURE M; CRONISTER A DIRECT MUTATION ANALYSIS OF 495 PATIENTS FOR FRAGILE-X CARRIER STATUS PROBAND DIAGNOSIS | 4 | 6 |
| 1238 | 11 | 13 | 1294 1995 AMERICAN JOURNAL OF MEDICAL GENETICS 55(3):384-386 PRIOR TW; PAPP AC; SNYDER PJ; SEDRA MS; GUIDA M; ENRILE BG GERMLINE MOSAICISM AT THE FRAGILE-X LOCUS | 2 | 7 |
| 1239 | 6 | 13 | 1395 1996 AMERICAN JOURNAL OF HUMAN GENETICS 58(3):641-643 Brown WT; Zhong N; Dobkin C Positive fragile X microsatellite associations point to a common mechanism of dynamic mutation evolution | 6 | 12 |
| 1240 | 7 | 13 | 1423 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):274-277 Steyaert J; Borghgraef M; Legius E; Fryns JP Molecular-intelligence correlations in young fragile X males with a mild CGG repeat expansion in the FMR1 gene | 15 | 19 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1241 | 4 | 13 | 1458 1996 ARCHIVES OF MEDICAL RESEARCH 27(4):587-588 Rivera H Fragile X studies and authorship | 1 | 5 |
| 1242 | 10 | 13 | 1491 1996 JOURNAL OF MEDICAL GENETICS 33(4):338-340 Mila M; CastellviBel S; Sanchez A; Lazaro C; Villa M; Estivill X Mosaicism for the fragile X syndrome full mutation and deletions within the CGG repeat of the FMR1 gene | 9 | 15 |
| 1243 | 8 | 13 | 1556 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 |
| 1244 | 2 | 13 | 1700 1998 STEROIDS 63(1):2-4 Joseph DR The rat androgen-binding protein (ABP/SHBG) gene contains triplet repeats similar to unstable triplets: Evidence that the ABP/SHBG and the fragile X-related 2 genes overlap | 0 | 8 |
| 1245 | 4 | 13 | 1730 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):296-297 Ferri R; Del Gracco S; Elia M; Musumeci SA; Pettinato S Heart rate variability and autonomic function during sleep in fragile X syndrome | 0 | 0 |
| 1246 | 3 | 13 | 1759 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):309-310 Zhong N; Ju WN; Brown WT; Ye LL; Jenkins EC; Schupf N Distribution of apolipoprotein E genotypes in fragile X syndrome and Batten disease | 0 | 0 |
| 1247 | 5 | 13 | 1760 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 85(3):197-201 Freedenberg DL; Gane LW; Richards CS; Lampe M; Hills J; O'Connor R; Manchester D; Taylor A; Tassone F; Hulseberg D; Hagerman RJ; Patil SR Fragile X syndrome and an isodicentric X chromosome in a woman with multiple anomalies, developmental delay, and normal pubertal development | 1 | 1 |
| 1248 | 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 |
| 1249 | 4 | 13 | 1952 2000 NEUROBIOLOGY OF LEARNING AND MEMORY 73(1):87-93 Irwin SA; Swain RA; Christmon CA; Chakravarti A; Weiler IJ; Greenough WT Evidence for altered Fragile-X mental retardation protein expression in response to behavioral stimulation | 20 | 25 |
| 1250 | 2 | 13 | 2043 2001 MOLECULAR AND CELLULAR ENDOCRINOLOGY 183:S77-S85 Sermon K; Seneca S; De Rycke M; Goossens V; Van de Velde H; De Vos A; Platteau P; Lissens W; Van Steirteghem A; Liebaers I PGD in the lab for triplet repeat diseases - myotonic dystrophy, Huntington's disease and Fragile-X syndrome | 0 | 9 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1251 | 10 | 13 | 2074 2001 SCIENCE 294(5551):2487-2488 Moine H; Mandel JL Biomedicine - Do G quartets orchestrate fragile X pathology? | 3 | 8 |
| 1252 | 9 | 13 | 2161 2002 MICROSCOPY RESEARCH AND TECHNIQUE 57(3):131-134 Kaufmann WE Neurobiology of fragile X syndrome: From molecular genetics to neurobehavioral phenotype | 0 | 2 |
| 1253 | 1 | 12 | 65 1982 HUMAN GENETICS 62(3):282-284 HOWELL RT; MCDERMOTT A REPLICATION STATUS OF THE FRAGILE X-CHROMOSOME, FRA(X) (Q27), IN 3 HETEROZYGOUS FEMALES | 21 | 30 |
| 1254 | 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 |
| 1255 | 1 | 12 | 171 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):123-131 HAGERMAN RJ; SYNHORST DP MITRAL-VALVE PROLAPSE AND AORTIC DILATATION IN THE FRAGILE-X SYNDROME | 9 | 17 |
| 1256 | 8 | 12 | 185 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(4):853-855 GARDNER RJM FRAGILE-X MALES WITH NORMAL INTELLIGENCE - AND IF SO, WHY | 4 | 7 |
| 1257 | 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 |
| 1258 | 4 | 12 | 247 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 |
| 1259 | 6 | 12 | 329 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):291-296 WELLS TE; MADISON LS ASSESSMENT OF BEHAVIOR-CHANGE IN A FRAGILE-X SYNDROME MALE TREATED WITH FOLIC-ACID | 3 | 5 |
| 1260 | 4 | 12 | 336 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):393-401 REISS AL; FEINSTEIN C; TOOMEY KE; GOLDSMITH B; ROSENBAUM K; CARUSO MA PSYCHIATRIC DISABILITY ASSOCIATED WITH THE FRAGILE-X CHROMOSOME | 29 | 44 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1261 | 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 |
| 1262 | 5 | 12 | 400 1986 LANCET 2(8517):1191-1192 [Anon] PREVENTIVE SCREENING FOR FRAGILE-X SYNDROME | 0 | 0 |
| 1263 | 10 | 12 | 460 1987 HUMAN GENETICS 77(3):297-298 WINTER R; PEMBREY M INTERPRETATION OF THE HETEROGENEITY IN THE LINKAGE RELATIONSHIPS OF DNA MARKERS AROUND THE FRAGILE-X LOCUS | 2 | 3 |
| 1264 | 8 | 12 | 548 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):673-679 HOLMGREN G; BLOMQUIST HK; DRUGGE U; GUSTAVSON KH FRAGILE-X FAMILIES IN A NORTHERN SWEDISH COUNTY - A GENEALOGICAL STUDY DEMONSTRATING APPARENT PATERNAL TRANSMISSION FROM THE 18TH-CENTURY | 10 | 10 |
| 1265 | 5 | 12 | 555 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 31(4):753-765 SHERMAN SL; ROGATKO A; TURNER G RECURRENCE RISKS FOR RELATIVES IN FAMILIES WITH AN ISOLATED CASE OF THE FRAGILE X SYNDROME | 11 | 15 |
| 1266 | 5 | 12 | 557 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 31(4):775-778 BUTLER MG; DEV VG; SHAH D; ULM JE; WILMOT PL; SHAPIRO LR THE USE OF EARLY SIMULTANEOUS PERCUTANEOUS UMBILICAL BLOOD-SAMPLING (PUBS) AND AMNIOCENTESIS FOR PRENATAL FRAGILE-X CHROMOSOME DIAGNOSIS | 0 | 0 |
| 1267 | 1 | 12 | 698 1990 CYTOMETRY 11(1):73-79 PIPER J; FANTES J; GOSDEN J; JI L AUTOMATIC DETECTION OF FRAGILE X-CHROMOSOMES USING AN X-CENTROMERE PROBE | 0 | 4 |
| 1268 | 6 | 12 | 700 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 |
| 1269 | 7 | 12 | 823 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):505-508 BRAINARD SS; SCHREINER RA; HAGERMAN RJ COGNITIVE PROFILES OF THE CARRIER FRAGILE-X WOMAN | 20 | 24 |
| 1270 | 2 | 12 | 830 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 41(3):275-278 LACHIEWICZ AM; HOEGERMAN SF; HOLMGREN G; HOLMBERG E; ARINBJARNARSON K ASSOCIATION OF THE ROBIN SEQUENCE WITH THE FRAGILE-X SYNDROME | 5 | 8 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1271 | 3 | 12 | 883 1991 NATURE 349(6312):742-743 CRAIG I HUMAN-GENETICS - METHYLATION AND THE FRAGILE-X | 1 | 5 |
| 1272 | 4 | 12 | 912 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):65-71 SUDHALTER V; MARANION M; BROOKS P EXPRESSIVE SEMANTIC DEFICIT IN THE PRODUCTIVE LANGUAGE OF MALES WITH FRAGILE-X SYNDROME | 18 | 20 |
| 1273 | 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 |
| 1274 | 11 | 12 | 929 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 |
| 1275 | 1 | 12 | 949 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):505-509 CIANCHETTI C; SANNIOFANCELLO G; FRATTA AL; PISCHEDDA MP; SPINICCI G; MARROSU MG; FILIPPI G NEUROPSYCHOLOGICAL STUDIES IN FAMILIES WITH FRAGILE-X NEGATIVE X-LINKED MENTAL-RETARDATION | 0 | 1 |
| 1276 | 7 | 12 | 1117 1993 JOURNAL OF MEDICAL GENETICS 30(6):454-459 JACOBS PA; BULLMAN H; MACPHERSON J; YOUINGS S; ROONEY V; WATSON A; DENNIS NR POPULATION STUDIES OF THE FRAGILE-X - A MOLECULAR APPROACH | 46 | 79 |
| 1277 | 3 | 12 | 1142 1993 NEUROPEDIATRICS 24(4):211-213 REES M; DIEBOLD U; PARKER K; DOOSE H; GARDINER RM; WHITEHOUSE WP BENIGN CHILDHOOD EPILEPSY WITH CENTROTEMPORAL SPIKES AND THE FOCAL SHARP WAVE TRAIT IS NOT LINKED TO THE FRAGILE-X REGION | 6 | 23 |
| 1278 | 6 | 12 | 1240 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 |
| 1279 | 8 | 12 | 1374 1995 JOURNAL OF MEDICAL GENETICS 32(11):907-908 PINTADO E; DEDIEGO Y; HMADCHA A; CARRASCO M; SIERRA J; LUCAS M INSTABILITY OF THE CGG REPEAT AT THE FRAXA LOCUS AND VARIABLE PHENOTYPIC-EXPRESSION IN A LARGE FRAGILE-X PEDIGREE | 2 | 9 |
| 1280 | 11 | 12 | 1408 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):176-180 Perroni L; Grasso M; Argusti A; LoNigro C; Croci GF; Zelante L; Garani GP; Bricarelli FD Molecular and cytogenetic analysis of the fragile X syndrome in a series of 453 mentally retarded subjects: A study of 87 families | 5 | 6 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1281 | 10 | 12 | 1409 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):181-183 Spence WC; Black SH; Fallon L; Maddalena A; Cummings E; MenapaceDrew G; Bick DP; Levinson G; Schulman JD; HowardPeebles PN Molecular fragile X screening in normal populations | 13 | 17 |
| 1282 | 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 |
| 1283 | 5 | 12 | 1614 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 |
| 1284 | 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 |
| 1285 | 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 |
| 1286 | 5 | 12 | 1763 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 87(4):366-368 Torrioli MG; Vernacotola S; Mariotti P; Bianchi E; Calvani M; De Gaetano A; Chiurazzi P; Neri G Double-blind, placebo-controlled study of L-acetylcarnitine for the treatment of hyperactive behavior in fragile X syndrome | 3 | 5 |
| 1287 | 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 |
| 1288 | 11 | 12 | 1892 2000 HUMAN GENETICS 106(3):366-369 Arocena DG; de Diego Y; Oostra BA; Willemsen R; Rodriguez MM A fragile X case with an amplification/deletion mosaic pattern | 0 | 0 |
| 1289 | 2 | 12 | 2064 2001 REVISTA DE NEUROLOGIA 33:S37-S41 Carrasco M Informing members of families affected by fragile X syndrome of this diagnosis | 0 | 0 |
| 1290 | 2 | 12 | 2243 2003 ARCHIVES OF NEUROLOGY 60(9):1197-1200 Kalidas S; Smith DP Functional genomics, fragile X syndrome, and RNA interference | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1291 | 2 | 11 | 116 1983 BRITISH JOURNAL OF PSYCHIATRY 143(SEP):256-260 GILLBERG C IDENTICAL TRIPLETS WITH INFANTILE-AUTISM AND THE FRAGILE-X SYNDROME | 20 | 38 |
| 1292 | 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 |
| 1293 | 0 | 11 | 144 1983 JOURNAL OF MEDICAL GENETICS 20(4):280-285 HARRISON CJ; JACK EM; ALLEN TD; HARRIS R THE FRAGILE X - A SCANNING ELECTRON-MICROSCOPE STUDY | 27 | 54 |
| 1294 | 2 | 11 | 179 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):255-257 DANIEL A; EKBLOM L; PHILLIPS S FRAGILE-X EXPRESSION SUPPRESSED IN EITHER FUDR OR METHOTREXATE TREATED FIBROBLASTS BY PRETREATMENT WITH 5-AZACYTIDINE | 3 | 5 |
| 1295 | 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 |
| 1296 | 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 |
| 1297 | 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 |
| 1298 | 2 | 11 | 219 1984 JOURNAL OF NERVOUS AND MENTAL DISEASE 172(9):549-551 KERBESHIAN J; BURD L; MARTSOLF J A FAMILY WITH FRAGILE-X SYNDROME | 7 | 20 |
| 1299 | 6 | 11 | 225 1984 NEW ENGLAND JOURNAL OF MEDICINE 310(22):1462-1462 WATSON MS; LECKMAN JF; ANNEX B; BREG WR; BOLES D; VOLKMAR FR; COHEN DJ; CARTER C FRAGILE X IN A SURVEY OF 75 AUTISTIC MALES | 34 | 56 |
| 1300 | 3 | 11 | 227 1984 OBSTETRICS AND GYNECOLOGY 63(3):S19-S21 HOGGE WA; SCHONBERG SA; GLOVER TW; HECHT F; GOLBUS MS PRENATAL-DIAGNOSIS OF FRAGILE (X) SYNDROME | 7 | 14 |
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