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Nodes: 2369
Authors: 4634,
Journals: 373,
Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by journal name.
Page 7: 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 |
|---|---|---|---|---|---|
| 601 | 17 | 38 | 951 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(6):1050-1056 GLASS IA; DELMASTRO RG; LANYON WG; RAEBURN JA; KILPATRICK MW; WEBB TP; CONNOR JM TIGHTLY LINKED POLYMORPHIC MARKERS FOR FRAGILE X-SYNDROME AND PRENATAL CYTOGENETIC DIAGNOSTIC EXPERIENCE | 0 | 0 |
| 602 | 7 | 15 | 952 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(6):1057-1062 WEBB T DELAYED REPLICATION OF XQ27 IN INDIVIDUALS WITH THE FRAGILE X-SYNDROME | 2 | 16 |
| 603 | 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 |
| 604 | 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 |
| 605 | 16 | 32 | 955 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 44(6):816-821 DEWALD GW; BUCKLEY DD; SPURBECK JL; JALAL SM CYTOGENETIC GUIDELINES FOR FRAGILE-X STUDIES TESTED IN ROUTINE PRACTICE | 3 | 7 |
| 606 | 18 | 21 | 956 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 44(6):830-833 MALMGREN H; GUSTAVSON KH; WAHLSTROM J; ARPIHENRIKSSON I; BENSCH J; PETTERSSON U; DAHL N INFANTILE-AUTISM FRAGILE-X - MOLECULAR FINDINGS SUPPORT GENETIC-HETEROGENEITY | 3 | 6 |
| 607 | 5 | 23 | 1059 1993 AMERICAN JOURNAL OF MEDICAL GENETICS 45(1):81-87 BERRYKRAVIS E; SKLENA P DEMONSTRATION OF ABNORMAL CYCLIC-AMP PRODUCTION IN PLATELETS FROM PATIENTS WITH FRAGILE-X SYNDROME | 11 | 14 |
| 608 | 13 | 25 | 1060 1993 AMERICAN JOURNAL OF MEDICAL GENETICS 45(5):589-593 MILUNSKY A; HUANG XL; AMOS JA; HERSKOWITZ J; FARRER LA; WYANDT HE 46,XY/47,XYY MALE WITH THE FRAGILE X-SYNDROME - CYTOGENETIC AND MOLECULAR STUDIES | 3 | 4 |
| 609 | 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 |
| 610 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 611 | 12 | 15 | 1063 1993 AMERICAN JOURNAL OF MEDICAL GENETICS 46(6):687-688 LAIRD CD IMPRINTING AND IMPRINT ERASURE AS VIEWED THROUGH THE FRAGILE-X SYNDROME | 2 | 5 |
| 612 | 4 | 9 | 1064 1993 AMERICAN JOURNAL OF MEDICAL GENETICS 47(2):216-220 WIEGERS AM; CURFS LMG; VERMEER ELMH; FRYNS JP ADAPTIVE-BEHAVIOR IN THE FRAGILE X-SYNDROME - PROFILE AND DEVELOPMENT | 5 | 6 |
| 613 | 60 | 138 | 1065 1993 AMERICAN JOURNAL OF MEDICAL GENETICS 48(2):112-121 FISCH GS WHAT IS ASSOCIATED WITH THE FRAGILE-X SYNDROME | 21 | 34 |
| 614 | 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 |
| 615 | 19 | 24 | 1153 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):281-293 SUTHERLAND GR; BROWN WT; HAGERMAN R; JENKINS E; LUBS H; MANDEL JL; NELSON D; NERI G; PARTINGTON MW; RICHARDS RI; STEVENSON R; TURNER G SIXTH INTERNATIONAL WORKSHOP ON THE FRAGILE-X AND X-LINKED MENTAL-RETARDATION | 3 | 4 |
| 616 | 8 | 22 | 1154 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):294-297 ALBRIGHT SG; LACHIEWICZ AM; TARLETON JC; RAO KW; SCHWARTZ CE; RICHIE R; TENNISON MB; AYLSWORTH AS FRAGILE-X PHENOTYPE IN A PATIENT WITH A LARGE DE-NOVO DELETION IN XQ27-Q28 | 10 | 17 |
| 617 | 38 | 61 | 1155 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):298-308 HAGERMAN RJ; HULL CE; SAFANDA JF; CARPENTER I; STALEY LW; OCONNOR RA; SEYDEL C; MAZZOCCO MMM; SNOW K; THIBODEAU SN; KUHL D; NELSON DL; CASKEY CT; TAYLOR AK HIGH FUNCTIONING FRAGILE-X MALES - DEMONSTRATION OF AN UNMETHYLATED FULLY EXPANDED FMR-1 MUTATION ASSOCIATED WITH PROTEIN EXPRESSION | 67 | 95 |
| 618 | 17 | 32 | 1156 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):309-314 CHIURAZZI P; DEGRAAFF E; NG J; VERKERK AJMH; WOLFSON S; FISCH GS; KOZAK L; NERI G; OOSTRA BA NO APPARENT INVOLVEMENT OF THE FMR1 GENE IN 5 PATIENTS WITH PHENOTYPIC MANIFESTATIONS OF THE FRAGILE-X-SYNDROME | 6 | 10 |
| 619 | 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 |
| 620 | 31 | 61 | 1158 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):317-327 ABRAMS MT; REISS AL; FREUND LS; BAUMGARDNER TL; CHASE GA; DENCKLA MB MOLECULAR-NEUROBEHAVIORAL ASSOCIATIONS IN FEMALES WITH THE FRAGILE-X FULL MUTATION | 48 | 65 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 621 | 26 | 42 | 1159 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):328-338 KOLEHMAINEN K; KARANT Y MODELING METHYLATION AND IQ SCORES IN FRAGILE-X FEMALES AND MOSAIC MALES | 4 | 7 |
| 622 | 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 |
| 623 | 16 | 34 | 1161 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):346-352 FISCH GS; HOLDEN JJA; SIMENSEN R; CARPENTER N; HOWARDPEEBLES PN; MADDALENA A; SANDGRUND A; JACQUES JR; MCGANN B FRAGILE-X-SYNDROME A PERVASIVE DEVELOPMENTAL DISABILITY - COGNITIVE-ABILITY AND ADAPTIVE-BEHAVIOR IN MATES WITH THE FULL MUTATION | 10 | 12 |
| 624 | 9 | 16 | 1162 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):353-357 FISCH GS; SIMENSEN R; ARINAMI T; BORGHGRAEF M; FRYNS JP LONGITUDINAL CHANGES IN IQ AMONG FRAGILE-X FEMALES - A PRELIMINARY MULTICENTER ANALYSIS | 9 | 10 |
| 625 | 14 | 36 | 1163 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):358-363 HAY DA DOES IQ DECLINE WITH AGE IN FRAGILE-X A METHODOLOGICAL CRITIQUE | 12 | 13 |
| 626 | 13 | 26 | 1164 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):364-369 LACHIEWICZ AM; DAWSON DV BEHAVIOR PROBLEMS OF YOUNG GIRLS WITH FRAGILE-X-SYNDROME - FACTOR SCORES ON THE CONNERS PARENTS QUESTIONNAIRE | 11 | 18 |
| 627 | 4 | 7 | 1165 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):370-373 STEYAERT J; DECRUYENAERE M; BORGHGRAEF M; FRYNS JP PERSONALITY PROFILE IN ADULT FEMALE FRAGILE-X CARRIERS - ASSESSED WITH THE MINNESOTA MULTIPHASIC PERSONALITY PROFILE (MMPI) | 3 | 8 |
| 628 | 3 | 6 | 1166 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):374-377 STEYAERT J; BORGHGRAEF M; FRYNS JP APPARENTLY ENHANCED VISUAL INFORMATION-PROCESSING IN FEMALE FRAGILE-X CARRIERS - PRELIMINARY FINDINGS | 1 | 1 |
| 629 | 17 | 44 | 1167 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):378-385 SOBESKY WE; PENNINGTON BF; PORTER D; HULL CE; HAGERMAN RJ EMOTIONAL AND NEUROCOGNITIVE DEFICITS IN FRAGILE-X | 25 | 30 |
| 630 | 9 | 30 | 1168 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):386-391 EINFELD SL; TONGE BJ; FLORIO T BEHAVIORAL AND EMOTIONAL DISTURBANCE IN FRAGILE-X-SYNDROME | 12 | 23 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 631 | 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 |
| 632 | 1 | 9 | 1170 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):400-402 SCHWARTZ CE; DEAN J; HOWARDPEEBLES PN; BUGGE M; MIKKELSEN M; TOMMERUP N; HULL C; HAGERMAN R; HOLDEN JJA; STEVENSON RE OBSTETRICAL AND GYNECOLOGICAL COMPLICATIONS IN FRAGILE-X CARRIERS - A MULTICENTER STUDY | 50 | 84 |
| 633 | 4 | 7 | 1171 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):403-404 SCHAAP C; FRYNS JP SEVERE PROGRESSIVE NEUROLOGICAL DISORDER ASSOCIATED WITH HYDROCEPHALUS IN A MAN WITH FRAGILE-X-SYNDROME | 1 | 2 |
| 634 | 11 | 25 | 1172 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):405-411 ZHONG N; YE LL; DOBKIN C; BROWN WT FRAGILE-X FOUNDER CHROMOSOME EFFECTS - LINKAGE DISEQUILIBRIUM OR MICROSATELLITE HETEROGENEITY | 17 | 29 |
| 635 | 15 | 17 | 1173 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):428-435 KOLEHMAINEN K POPULATION-GENETICS OF FRAGILE-X - A MULTIPLE ALLELE MODEL WITH VARIABLE RISK OF CGG REPEAT EXPANSION | 15 | 21 |
| 636 | 5 | 8 | 1174 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):436-442 JENKINS EC; MORYS I; HENDERSON J; GENOVESE M; CARTER M; LI SY; HOUCK GE; DING XH; STARKHOUCK SL; DOBKIN CS; BROWN WT FRAGILE-X INDUCTION SYSTEMS IN CVS CULTURES - EFFECT ON CYTOGENETIC, PCR, AND GENOMIC SOUTHERN BLOT DNA ANALYSES OF THE FMR-1 GENE | 1 | 1 |
| 637 | 4 | 15 | 1175 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):447-450 POMPONI MG; NERI G BUTYRATE AND ACETYL-CARNITINE INHIBIT THE CYTOGENETIC EXPRESSION OF THE FRAGILE-X IN-VITRO | 1 | 6 |
| 638 | 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 |
| 639 | 7 | 8 | 1177 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):452-453 JENKINS EC; GENOVESE M; DUNCAN CJ; GU H; STARKHOUCK S; LI SY; HENDERSON J; MORYS I; BROWN WT OCCURRENCE OF ANEUPLOIDY FOR THE X-CHROMOSOME IN OVER 1,300 UNRELATED SPECIMENS SCREENED FOR THE FRAGILE X-CHROMOSOME | 1 | 1 |
| 640 | 12 | 16 | 1178 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):454-457 TROTTIER Y; IMBERT G; POUSTKA A; FRYNS JP; MANDEL JL MALE WITH TYPICAL FRAGILE-X PHENOTYPE IS DELETED FOR PART OF THE FMR1 GENE AND FOR ABOUT 100 KB OF UPSTREAM REGION | 15 | 27 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 641 | 15 | 19 | 1179 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):458-462 TURNER AM; ROBINSON H; WAKE S; LAING SJ; LEIGH D; TURNER G COUNSELING RISK FIGURES FOR FRAGILE-X CARRIER FEMALES OF VARYING BAND SIZES FOR USE IN PREDICTING THE LIKELIHOOD OF RETARDATION IN THEIR OFFSPRING | 5 | 8 |
| 642 | 7 | 10 | 1180 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):463-465 RYYNANEN M; PULKKINEN L; KIRKINEN P; SAARIKOSKI S FRAGILE-X SYNDROME IN EAST FINLAND - MOLECULAR APPROACH TO GENETIC AND PRENATAL-DIAGNOSIS | 3 | 4 |
| 643 | 15 | 21 | 1181 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):466-470 HOFSTEE Y; ARINAMI T; HAMAGUCHI H COMPARISON BETWEEN THE CYTOGENETIC TEST FOR FRAGILE-X AND THE MOLECULAR ANALYSIS OF THE FMR-1 GENE IN JAPANESE MENTALLY-RETARDED INDIVIDUALS | 12 | 18 |
| 644 | 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 |
| 645 | 27 | 37 | 1183 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):474-481 HAGERMAN RJ; WILSON P; STALEY LW; LANG KA; FAN T; UHLHORN C; JEWELLSMART S; HULL C; DRISKO J; FLOM K; TAYLOR AK EVALUATION OF SCHOOL-CHILDREN AT HIGH-RISK FOR FRAGILE-X-SYNDROME UTILIZING BUCCAL CELL FMR-1 TESTING | 17 | 36 |
| 646 | 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 |
| 647 | 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 |
| 648 | 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 |
| 649 | 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 |
| 650 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 651 | 16 | 17 | 1189 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):509-512 NOLIN SL; GLICKSMAN A; HOUCK GE; BROWN WT; DOBKIN CS MOSAICISM IN FRAGILE-X AFFECTED MALES | 36 | 40 |
| 652 | 18 | 33 | 1190 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):517-521 CHIURAZZI P; KOZAK L; NERI G UNSTABLE TRIPLETS AND THEIR MUTATIONAL MECHANISM - SIZE-REDUCTION OF THE CGG REPEAT VS GERMLINE MOSAICISM IN THE FRAGILE-X-SYNDROME | 7 | 15 |
| 653 | 4 | 11 | 1191 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):522-526 CHONG SS; EICHLER EE; NELSON DL; HUGHES MR ROBUST AMPLIFICATION AND ETHIDIUM-VISIBLE DETECTION OF THE FRAGILE-X-SYNDROME CGG REPEAT USING PFU POLYMERASE | 19 | 41 |
| 654 | 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 |
| 655 | 0 | 0 | 1193 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):606-614 [Anon] ABSTRACTS FOR THE 6TH INTERNATIONAL WORKSHOP ON FRAGILE-X-SYNDROME AND X-LINKED MENTAL-RETARDATION | 0 | 0 |
| 656 | 14 | 17 | 1194 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 53(4):370-373 PUISSANT H; MALINGE MC; LARGETPIET A; MARTIN D; CHAUVEAU P; ODENT S; PLESSIS G; PARENT P; LEMAREC B; LARGETPIET L MOLECULAR ANALYSIS OF 53 FRAGILE-X FAMILIES WITH THE PROBE-STB12.3 | 1 | 2 |
| 657 | 1 | 2 | 1195 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 53(4):380-381 PARK V; HOWARDPEEBLES P; SHERMAN S; TAYLOR A; WULFSBERG E POLICY STATEMENT - AMERICAN-COLLEGE-OF-MEDICAL-GENETICS - FRAGILE-X-SYNDROME - DIAGNOSTIC AND CARRIER TESTING | 16 | 27 |
| 658 | 0 | 3 | 1196 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 53(4):382-382 HOWARDPEEBLES PN; MADDALENA A; SPENCE WC; LEVINSON G; FALLON L; BICK DP; BLACK SH; SCHULMAN JD FRAGILE-X SCREENING - WHAT IS THE REAL ISSUE | 5 | 9 |
| 659 | 9 | 28 | 1197 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 54(2):141-143 CRADDOCK N; DANIELS J; MCGUFFIN P; OWEN M VARIATION AT THE FRAGILE X-LOCUS DOES NOT INFLUENCE SUSCEPTIBILITY TO BIPOLAR DISORDER | 1 | 6 |
| 660 | 13 | 28 | 1198 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 54(4):378-383 THOMPSON NM; GULLEY ML; ROGENESS GA; CLAYTON RJ; JOHNSON C; HAZELTON B; CHO CG; ZELLMER VT NEUROBEHAVIORAL CHARACTERISTICS OF CGG AMPLIFICATION STATUS IN FRAGILE-X FEMALES | 17 | 26 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 661 | 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 |
| 662 | 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 |
| 663 | 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 |
| 664 | 14 | 21 | 1297 1995 AMERICAN JOURNAL OF MEDICAL GENETICS 59(4):426-430 MCCONKIEROSELL A; ROBINSON H; WAKE S; STALEY LW; HELLER K; CRONISTER A DISSEMINATION OF GENETIC RISK INFORMATION TO RELATIVES IN THE FRAGILE-X SYNDROME - GUIDELINES FOR GENETIC COUNSELORS | 6 | 7 |
| 665 | 1 | 9 | 1298 1995 AMERICAN JOURNAL OF MEDICAL GENETICS 59(4):526-526 SCHIANO CM; DEMB HB; BROWN WT LACK OF SIGNIFICANT ASSOCIATION BETWEEN SPINA-BIFIDA AND THE FRAGILE-X SYNDROME | 0 | 0 |
| 666 | 9 | 28 | 1299 1995 AMERICAN JOURNAL OF MEDICAL GENETICS 60(1):39-43 SPINELLI M; ROCHA ACD; GIACHETI CM; RICHIERICOSTA A WORD-FINDING DIFFICULTIES, VERBAL PARAPHASIAS, AND VERBAL DYSPRAXIA IN 10 INDIVIDUALS WITH FRAGILE-X-SYNDROME | 5 | 5 |
| 667 | 18 | 19 | 1300 1995 AMERICAN JOURNAL OF MEDICAL GENETICS 60(4):302-306 MUELLER OT; HARTSFIELD JK; AMAR MJA; GALLARDO LA; KOUSSEFF BG FRAGILE-X SYNDROME - DISCORDANT LEVELS OF CGG REPEAT MOSAICISM IN 2 BROTHERS | 2 | 5 |
| 668 | 28 | 92 | 1301 1995 AMERICAN JOURNAL OF MEDICAL GENETICS 60(6):480-493 Schapiro MB; Murphy DGM; Hagerman RJ; Azari NP; Alexander GE; Miezejeski CM; Hinton VJ; Horwitz B; Haxby JV; Kumar A; White B; Grady CL Adult fragile X syndrome: Neuropsychology, brain anatomy, and metabolism | 19 | 29 |
| 669 | 11 | 24 | 1398 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 63(2):396-400 Giampietro PF; Haas BR; Lipper E; Gutman A; Zellers NJ; LaTrenta GS; Brooks SS; Matalon R; Kaul R; Ding XH; Brown WT Fragile X syndrome in two siblings with major congenital malformations | 0 | 1 |
| 670 | 0 | 0 | 1399 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):1-1 Laing S; Robinson H; Wake S; Wright F; Turner G Normal males and their role in transmission of the fragile x syndrome. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 671 | 15 | 34 | 1400 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):1-14 Tranebjaerg L; Lubs HA; Borghgraef M; Brown WT; Fisch G; Fryns JP; Hagerman R; Jacobs PA; Mandel JL; Mulley J; Oostra B; Schwartz C; Sherman S; Willard H; Willems P Seventh International Workshop on the Fragile X and X-linked Mental Retardation | 2 | 4 |
| 672 | 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 |
| 673 | 0 | 0 | 1402 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):14-14 Malzac P; Biancalana V; Voelckel MA; Moncla A; Pellissier MC; Boccaccio I; Mandel JL; Mattei JF A rare example of a reverse mutation in a fragile X syndrome family. | 0 | 0 |
| 674 | 0 | 0 | 1403 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):16-16 Murray A; Conway GS; Jacobs PA Premature ovarian failure and fragile X. | 0 | 0 |
| 675 | 0 | 0 | 1404 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):17-17 Oostra BA; Willemsen R; Mandel JL; DeVries B; Devys D Rapid screening test for fragile X syndrome. | 0 | 0 |
| 676 | 0 | 0 | 1405 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):19-19 Shen Y; Zhu N; Huang D; Wu GY Studies on fragile X syndrome in the Chinese. | 0 | 0 |
| 677 | 0 | 0 | 1406 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):25-25 deVries BBA; vandenOuweland AMW; Mohkamsing S; Halley DJJ; Tibben A; Oostra BA; Galjaard H; Niermeijer MF Acceptance of screening for the fragile X syndrome among 1878 mentally retarded individuals in institutions and special schools in the Netherlands | 0 | 0 |
| 678 | 4 | 21 | 1407 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):27-30 Carrel L; Willard HF An assay for X inactivation based on differential methylation at the fragile X locus, FMR1 | 1 | 30 |
| 679 | 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 |
| 680 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 681 | 9 | 10 | 1410 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):187-190 Grasso M; Perroni L; Colella S; Piombo G; Argusti A; Lituania M; Buscaglia M; Giussani U; Grimoldi MG; Bricarelli FD Prenatal diagnosis of 30 fetuses at risk for fragile X syndrome | 1 | 2 |
| 682 | 16 | 24 | 1411 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):191-195 Brown WT; Nolin S; Houck G; Ding XH; Glicksman A; Li SY; StarkHouck S; Brophy P; Duncan C; Dobkin C; Jenkins E Prenatal diagnosis and carrier screening for fragile X by PCR | 16 | 25 |
| 683 | 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 |
| 684 | 4 | 11 | 1413 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):198-202 Robinson H; Wake S; Wright F; Laing S; Turner G Informed choice in fragile X syndrome and its effects on prevalence | 9 | 11 |
| 685 | 30 | 50 | 1414 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):203-208 Chiurazzi P; Macpherson J; Sherman S; Neri G Significance of linkage disequilibrium between the fragile X locus and its flanking markers | 9 | 23 |
| 686 | 24 | 59 | 1415 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):209-215 Chiurazzi P; Genuardi M; Kozak L; GiovannucciUzielli ML; Bussani C; DagnaBricarelli F; Grasso M; Perroni L; Sebastio G; Sperandeo MP; Oostra BA; Neri G Fragile X founder chromosomes in Italy: A few initial events and possible explanation for their heterogeneity | 11 | 24 |
| 687 | 28 | 43 | 1416 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):226-233 Zhong N; Kajanoja E; Smits B; Pietrofesa J; Curley D; Wang DW; Ju MN; Nolin S; Dobkin C; Ryynanen M; Brown WT Fragile X founder effects and new mutations in Finland | 9 | 24 |
| 688 | 13 | 20 | 1417 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):234-238 Syrrou M; Patsalis PC; Georgiou I; Hadjimarcou MI; ConstantinouDeltas CD; Pagoulatos G Evidence for high-risk haplotypes and (CGG)n expansion in fragile X syndrome in the Hellenic population of Greece and Cyprus | 5 | 15 |
| 689 | 10 | 20 | 1418 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):241-245 Kooy RF; DHooge R; Reyniers E; Bakker CE; Nagels G; DeBoulle K; Storm K; Clincke G; DeDeyn PP; Oostra BA; Willems PJ Transgenic mouse model for the fragile X syndrome | 22 | 41 |
| 690 | 13 | 37 | 1419 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):246-251 Godfraind JM; Reyniers E; DeBoulle K; DHooge R; DeDeyn PP; Bakker CE; Oostra BA; Kooy RF; Willems PJ Long-term potentiation in the hippocampus of fragile X knockout mice | 22 | 31 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 691 | 17 | 21 | 1420 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):256-260 Sherman SL; Meadows KL; Ashley AE Examination of factors that influence the expansion of the fragile X mutation in a sample of conceptuses from known carrier females | 12 | 16 |
| 692 | 19 | 28 | 1421 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):261-265 Zhong N; Ju WN; Pietrofesa J; Wang DW; Dobkin C; Brown WT Fragile X ''gray zone'' alleles: AGG patterns, expansion risks, and associated haplotypes | 15 | 26 |
| 693 | 5 | 21 | 1422 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):266-267 Wohrle D; Schwemmle S; Steinbach P DNA methylation and triplet repeat stability: New proposals addressing actual questions on the CGG repeat of fragile X syndrome | 9 | 18 |
| 694 | 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 |
| 695 | 12 | 21 | 1424 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):278-282 Lachiewicz AM; Spiridigliozzi GA; McConkieRosell A; Burgess D; Feng Y; Warren ST; Tarleton J A fragile X male with a broad smear on Southern blot analysis representing 100-500 CGG repeats and no methylation at the EagI site of the FMR-1 gene | 9 | 11 |
| 696 | 21 | 35 | 1425 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):287-292 Brown WT; Houck GE; Ding XH; Zhong N; Nolin S; Glicksman A; Dobkin C; Jenkins EC Reverse mutations in the fragile X syndrome | 9 | 18 |
| 697 | 16 | 20 | 1426 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):293-295 Mannermaa A; Pulkkinen L; Kajanoja E; Ryynanen M; Saarikoski S Deletion in the FMR1 gene in a fragile-X male | 8 | 9 |
| 698 | 17 | 24 | 1427 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):296-301 Dobkin CS; Nolin SL; Cohen I; Sudhalter V; Bialer MG; Ding XH; Jenkins EC; Zhong N; Brown WT Tissue differences in fragile X mosaics: Mosaicism in blood cells may differ greatly from skin | 9 | 11 |
| 699 | 29 | 43 | 1428 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):302-308 deGraaff E; deVries BBA; Willemsen R; vanHemel JO; Mohkamsing S; Oostra BA; vandenOuweland AMW The fragile X phenotype in a mosaic male with a deletion showing expression of the FMR1 protein in 28% of the cells | 11 | 13 |
| 700 | 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 |
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