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Nodes: 2369
Authors: 4634,
Journals: 373,
Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by journal name.
Page 6: 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 |
|---|---|---|---|---|---|
| 501 | 1 | 1 | 682 1990 AMERICAN JOURNAL OF MEDICAL GENETICS 37(3):434-434 MINGRONINETTO RC; ROSENBERG C; VIANNAMORGANTE AM; PAVANELLO RCM FRAGILE-X FREQUENCY - RESPONSE | 0 | 0 |
| 502 | 12 | 39 | 780 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):158-172 BROWN WT; JENKINS E; NERI G; LUBS H; SHAPIRO LR; DAVIES KE; SHERMAN S; HAGERMAN R; LAIRD C 4TH INTERNATIONAL WORKSHOP ON THE FRAGILE-X AND X-LINKED MENTAL-RETARDATION | 1 | 7 |
| 503 | 0 | 0 | 781 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):173-185 SPANO LM; OPITZ JM BIBLIOGRAPHY ON X-LINKED MENTAL-RETARDATION, THE FRAGILE-X, AND RELATED SUBJECTS .5. (1991) | 0 | 1 |
| 504 | 12 | 19 | 782 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):251-255 NOLIN SL; SNIDER DA; JENKINS EC; BROWN WT; KRAWCZUN M; STETKA D; HOUCK G; DOBKIN CS; STRONG G; SMITHDOBRANSKY G; VICTOR A; HUGHES K; KIMPTON D; LITTLE A; NAGARAJA U; KENEFICK B; SULLIVAN C FRAGILE-X SCREENING-PROGRAM IN NEW-YORK-STATE | 18 | 24 |
| 505 | 1 | 1 | 783 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):256-259 LAING S; PARTINGTON M; ROBINSON H; TURNER G CLINICAL SCREENING SCORE FOR THE FRAGILE-X (MARTIN-BELL) SYNDROME | 25 | 29 |
| 506 | 7 | 32 | 784 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):260-268 BUTLER MG; ALLEN GA; HAYNES JL; SINGH DN; WATSON MS; BREG WR ANTHROPOMETRIC COMPARISON OF MENTALLY-RETARDED MALES WITH AND WITHOUT THE FRAGILE-X SYNDROME | 16 | 22 |
| 507 | 11 | 14 | 785 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):269-274 CRONISTER A; SCHREINER R; WITTENBERGER M; AMIRI K; HARRIS K; HAGERMAN RJ HETEROZYGOUS FRAGILE-X FEMALE - HISTORICAL, PHYSICAL, COGNITIVE, AND CYTOGENETIC FEATURES | 36 | 54 |
| 508 | 12 | 21 | 786 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):283-287 HAGERMAN RJ; AMIRI K; CRONISTER A FRAGILE-X CHECKLIST | 45 | 60 |
| 509 | 1 | 8 | 787 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):288-289 ZHAO Y; SHEN Y; LIU Y; ZHANG JC; YE LZ; MA SW; LO WHY; WU GY; CHENG ZY; ZHANG XZ FRAGILE-X SYNDROME (MARTIN-BELL SYNDROME) IN CHINA | 0 | 1 |
| 510 | 12 | 23 | 788 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):292-297 BROWN WT; GROSS A; GOONEWARDENA P; FERRANDO C; DOBKIN C; JENKINS EC DETECTION OF FRAGILE-X NON-PENETRANT MALES BY DNA MARKER ANALYSIS | 4 | 4 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 511 | 16 | 47 | 789 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):298-304 GLASS IA; PIRRIT LA; WHITE EM; BELL MV; DAVIES KE; COCKBURN F; CONNOR JM LINKAGE ANALYSIS IN THE FRAGILE-X SYNDROME USING MULTIPLE DISTAL XQ POLYMORPHIC DNA MARKERS | 2 | 2 |
| 512 | 2 | 9 | 790 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):305-310 MURPHY PD; WATSON MS; SHAPIRO LR; WILMOT PL; BREG WR DNA-BASED GENETIC TESTING IN 50 FRAGILE-X FAMILIES | 2 | 2 |
| 513 | 7 | 20 | 791 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):311-318 CARPENTER NJ DNA LINKAGE ANALYSIS OF 26 FAMILIES WITH FRAGILE-X SYNDROME | 1 | 1 |
| 514 | 9 | 14 | 792 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):319-321 DAHL N; MALMGREN H; PETTERSSON U; HOLMGREN G; SEEMANOVA E; GUSTAVSON KH CARRIER DETECTION OF THE FRAGILE-X SYNDROME USING FLANKING LOCI DXS98, DXS105, AND DXS304 | 0 | 0 |
| 515 | 14 | 31 | 793 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):322-327 GOONEWARDENA P; BROWN WT; GROSS AC; FERRANDO C; DOBKIN C; ROMANO V; BOSCO P; CERATTO N; PETTERSSON U; DAHL N LINKAGE ANALYSIS OF THE FRAGILE-X SYNDROME USING A NEW DNA MARKER U6.2 DEFINING LOCUS DXS304 | 1 | 1 |
| 516 | 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 |
| 517 | 3 | 20 | 795 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):343-346 BROWN WT; GROSS AC; GOONEWARDENA P; FERRANDO C; DOBKIN C; JENKINS EC LINKAGE IN FRAGILE-X FAMILIES OF 3 DISTAL FLANKING MARKERS - ST14, DX13, AND F8 | 1 | 2 |
| 518 | 4 | 4 | 796 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):347-348 ROMANO V; MASCALI G; CHIAVETTA V; RAGUSA RM; BARLETTA C; ROMANO C; MOLLICA F; MATTINA T; GROSS A; BROWN WT; DOBKIN CS; FERRANDO C RFLP ANALYSIS IN 5 SICILIAN FAMILIES WITH THE FRAGILE-X SYNDROME | 0 | 0 |
| 519 | 16 | 20 | 797 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):349-353 CARPENTER NJ; THIBODEAU SN; BROWN WT LINKAGE RELATIONSHIPS BETWEEN DXS105, DXS98, AND OTHER POLYMORPHIC DNA MARKERS FLANKING THE FRAGILE-X LOCUS | 2 | 3 |
| 520 | 7 | 11 | 798 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):363-366 DRUGGE U; BLOMQUIST HK; GUSTAVSON KH; HOLMGREN G FRAGILE-X FAMILIES IN A NORTHERN SWEDISH COUNTY - A GENEALOGICAL STUDY OF POSSIBLY AFFECTED INDIVIDUALS IN THE 19TH-CENTURY | 2 | 2 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 521 | 12 | 18 | 799 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):367-369 PELLISSIER MC; VOELCKEL MA; PIQUET C; MATTEI MG; MATTEI JF TRANSMISSION OF MENTAL-RETARDATION WITH FRAGILE-X SITE BY 2 NORMAL TRANSMITTER BROTHERS | 0 | 0 |
| 522 | 13 | 23 | 800 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):370-373 BROOKS SS; COHEN I; FERRANDO C; JENKINS EC; BROWN WT; DOBKIN C CYTOGENETICALLY NEGATIVE, LINKAGE POSITIVE FRAGILE-X SYNDROME | 0 | 1 |
| 523 | 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 |
| 524 | 1 | 5 | 802 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):378-379 DOBKIN CS; DRISCOLL MC; FERRANDO C POLYMERASE CHAIN-REACTION DETECTION OF THE DDE-I POLYMORPHISM IN THE FACTOR-IX GENE FOR FRAGILE-X LINKAGE ANALYSIS | 0 | 3 |
| 525 | 4 | 15 | 803 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):380-383 PERGOLIZZI R; BROWN WT; GOONEWARDENA P; BHAN R; DOBKIN C; DAHL N; PETTERSSON U MOLECULAR CHARACTERIZATION OF A DNA PROBE, U6.2, LOCATED CLOSE TO THE FRAGILE-X LOCUS | 0 | 0 |
| 526 | 11 | 25 | 804 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):391-395 LAIRD CD POSSIBLE ERASURE OF THE IMPRINT ON A FRAGILE-X CHROMOSOME WHEN TRANSMITTED BY A MALE | 8 | 15 |
| 527 | 4 | 7 | 805 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):396-399 SHERMAN SL COLLABORATIVE PROSPECTIVE-STUDY OF THE FRAGILE-X SYNDROME - REQUEST FOR PARTICIPATION | 2 | 2 |
| 528 | 4 | 23 | 806 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):400-403 JACKY PB; AHUJA YR; ANYANEYEBOA K; BREG WR; CARPENTER NJ; FROSTERISKENIUS UG; FRYNS JP; GLOVER TW; GUSTAVSON KH; HOEGERMAN SF; HOLMGREN G; HOWARDPEEBLES PN; JENKINS EC; KRAWCZUN MS; NERI G; PETTIGREW A; SCHAAP T; SCHONBERG SA; SHAPIRO LR; SPINNER N; STEINBACH P; VIANNAMORGANTE AM; WATSON MS; WILMOT PL GUIDELINES FOR THE PREPARATION AND ANALYSIS OF THE FRAGILE-X CHROMOSOME IN LYMPHOCYTES | 31 | 44 |
| 529 | 7 | 16 | 807 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):404-407 FISCH GS; SILVERMAN W; JENKINS EC GENETIC AND OTHER FACTORS THAT CONTRIBUTE TO VARIABILITY IN CYTOGENETIC EXPRESSION IN FRAGILE-X MALES | 4 | 7 |
| 530 | 0 | 4 | 808 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):408-410 SHAPIRO LR; WILMOT PL; SHAPIRO DA; PETTERSEN IM; CASAMASSIMA AC CYTOGENETIC DIAGNOSIS OF THE FRAGILE-X SYNDROME - EFFICIENCY, UTILIZATION, AND TRENDS | 3 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 531 | 1 | 7 | 809 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):416-417 JENKINS LS; GRUENERT DC; JENKINS EC; SCHONBERG SA TRANSFORMATION AND ESTABLISHMENT OF FRAGILE-X CELL-LINES FROM AMNIOCYTES | 1 | 1 |
| 532 | 4 | 16 | 810 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):418-420 LEDBETTER SA; SCHWARTZ CE; DAVIES KE; LEDBETTER DH NEW SOMATIC-CELL HYBRIDS FOR PHYSICAL MAPPING IN DISTAL XQ AND THE FRAGILE-X REGION | 0 | 14 |
| 533 | 12 | 22 | 811 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):421-424 ROSENBERG C; VIANNAMORGANTE AM; OTTO PA; NAVAJAS L EFFECT OF X-INACTIVATION ON FRAGILE-X FREQUENCY AND MENTAL-RETARDATION | 3 | 5 |
| 534 | 6 | 20 | 812 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):429-433 KIMCHISARFATY C; GOITEIN R; KEREM B; WERNER M; MEIDAN B; SCHAAP T ENDOREDUPLICATION AND POLYPLOIDY IN FRAGILE-X CELLS INDUCED BY METHOTREXATE AND FLUORODEOXYURIDINE - IMPLICATIONS FOR DIAGNOSIS | 1 | 3 |
| 535 | 10 | 28 | 813 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):440-444 KUPKE KG; SORENG AL; MULLER U ORIGIN OF THE SUPERNUMERARY X-CHROMOSOME IN A PATIENT WITH FRAGILE-X AND KLINEFELTER SYNDROME | 7 | 9 |
| 536 | 2 | 4 | 814 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):445-446 HOWARDPEEBLES PN FRAGILE-X EXPRESSION - USE OF A DOUBLE INDUCTION SYSTEM | 2 | 4 |
| 537 | 4 | 11 | 815 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):453-455 SHAPIRO LR; WILMOT PL; MURPHY PD PRENATAL-DIAGNOSIS OF THE FRAGILE-X SYNDROME - POSSIBLE END OF THE EXPERIMENTAL PHASE FOR AMNIOTIC-FLUID | 5 | 6 |
| 538 | 2 | 33 | 816 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):456-463 KRAWCZUN MS; JENKINS EC; DUNCAN CJ; STARKHOUCK SL; KUNAPORN S; SCHWARTZRICHSTEIN C; HONG G; BROWN WT DISTRIBUTION OF AUTOSOMAL FRAGILE SITES IN SPECIMENS CULTURED FOR PRENATAL FRAGILE-X DIAGNOSIS | 1 | 1 |
| 539 | 1 | 8 | 817 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):464-466 JENKINS EC; BROOKS SE; STARKHOUCK SL; DUNCAN CJ; BROOKS SLS; BROWN WT SV40-TRANSFORMED FRAGILE(X) AMNIOCYTES | 1 | 1 |
| 540 | 9 | 34 | 818 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):481-487 FISCH GS; ARINAMI T; FROSTERISKENIUS U; FRYNS JP; CURFS LM; BORGHGRAEF M; HOWARDPEEBLES PN; SCHWARTZ CE; SIMENSEN RJ; SHAPIRO LR RELATIONSHIP BETWEEN AGE AND IQ AMONG FRAGILE-X MALES - A MULTICENTER STUDY | 13 | 14 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 541 | 6 | 20 | 819 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):488-492 DEVONFLINDT R; BYBEL B; CHUDLEY AE; LOPES F SHORT-TERM-MEMORY AND COGNITIVE VARIABILITY IN ADULT FRAGILE-X FEMALES | 6 | 8 |
| 542 | 3 | 21 | 820 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):493-497 SUDHALTER V; SCARBOROUGH HS; COHEN IL SYNTACTIC DELAY AND PRAGMATIC DEVIANCE IN THE LANGUAGE OF FRAGILE-X MALES | 21 | 29 |
| 543 | 3 | 19 | 821 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):498-502 COHEN IL; VIETZE PM; SUDHALTER V; JENKINS EC; BROWN WT EFFECTS OF AGE AND COMMUNICATION LEVEL ON EYE CONTACT IN FRAGILE-X MALES AND NON-FRAGILE-X AUTISTIC MALES | 22 | 33 |
| 544 | 7 | 15 | 822 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):503-504 CRONISTER A; HAGERMAN RJ; WITTENBERGER M; AMIRI K MENTAL IMPAIRMENT IN CYTOGENETICALLY POSITIVE FRAGILE-X FEMALES | 14 | 15 |
| 545 | 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 |
| 546 | 3 | 9 | 824 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):509-509 HECHT F SEIZURE DISORDERS IN THE FRAGILE-X CHROMOSOME SYNDROME | 3 | 7 |
| 547 | 3 | 10 | 825 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):511-513 MUSUMECI SA; FERRI R; ELIA M; COLOGNOLA RM; BERGONZI P; TASSINARI CA EPILEPSY AND FRAGILE-X SYNDROME - A FOLLOW-UP-STUDY | 21 | 36 |
| 548 | 5 | 15 | 826 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 39(3):374-375 MOORE PSJ; CHUDLEY AE; WINTER JSD PITUITARY-GONADAL AXIS IN PREPUBERTAL BOYS WITH THE FRAGILE-X SYNDROME | 5 | 7 |
| 549 | 14 | 31 | 827 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 40(2):234-243 CIANCHETTI C; SANNIOFANCELLO G; FRATTA AL; MANCONI F; ORANO A; PISCHEDDA MP; PRUNA D; SPINICCI G; ARCHIDIACONO N; FILIPPI G NEUROPSYCHOLOGICAL, PSYCHIATRIC, AND PHYSICAL MANIFESTATIONS IN 149 MEMBERS FROM 18 FRAGILE-X FAMILIES | 16 | 19 |
| 550 | 2 | 4 | 828 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 40(4):523-523 DREESEN JCFM; SMITS A; BRUNNER H RISK CALCULATIONS IN THE FRAGILE-X SYNDROME | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 551 | 2 | 5 | 829 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 40(4):524-524 WILLEMS PJ; VANROY B; RAEYMAEKERS P; OOSTRA B RISK CALCULATIONS IN THE FRAGILE-X SYNDROME - REPLY | 0 | 0 |
| 552 | 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 |
| 553 | 10 | 39 | 831 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 41(3):289-294 HINTON VJ; BROWN WT; WISNIEWSKI K; RUDELLI RD ANALYSIS OF NEOCORTEX IN 3 MALES WITH THE FRAGILE-X SYNDROME | 76 | 117 |
| 554 | 8 | 14 | 904 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 42(2):184-186 FINUCANE BM; JAEGER E; DUNN E; SCOTT CI STUDY OF COLOR-VISION IN FRAGILE-X SYNDROME | 1 | 1 |
| 555 | 8 | 19 | 905 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 42(6):835-838 RAMOS FJ; EMANUEL BS; SPINNER NB FREQUENCY OF THE COMMON FRAGILE SITE AT XQ27.2 UNDER CONDITIONS OF THYMIDYLATE STRESS - IMPLICATIONS FOR CYTOGENETIC DIAGNOSIS OF THE FRAGILE-X SYNDROME | 0 | 1 |
| 556 | 24 | 31 | 906 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):5-27 MANDEL JL; HAGERMAN R; FROSTER U; BROWN WT; JENKINS EC; JACOBS P; TURNER G; LUBS H; NERI G 5TH INTERNATIONAL WORKSHOP ON THE FRAGILE-X AND X-LINKED MENTAL-RETARDATION | 5 | 8 |
| 557 | 9 | 27 | 907 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):28-34 FISCH GS; SHAPIRO LR; SIMENSEN R; SCHWARTZ CE; FRYNS JP; BORGHGRAEF M; CURFS LM; HOWARDPEEBLES PN; ARINAMI T; MAVROU A LONGITUDINAL CHANGES IN IQ AMONG FRAGILE-X MALES - CLINICAL-EVIDENCE OF MORE THAN ONE MUTATION | 12 | 12 |
| 558 | 12 | 22 | 908 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):35-46 REISS AL; FREUND L BEHAVIORAL-PHENOTYPE OF FRAGILE-X SYNDROME - DSM-III-R AUTISTIC BEHAVIOR IN MALE-CHILDREN | 52 | 71 |
| 559 | 30 | 56 | 909 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):47-55 FISCH GS IS AUTISM ASSOCIATED WITH THE FRAGILE-X SYNDROME | 19 | 36 |
| 560 | 10 | 18 | 910 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):56-60 EINFELD S; HALL W BEHAVIOR PHENOTYPE OF THE FRAGILE X SYNDROME | 6 | 12 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 561 | 2 | 9 | 911 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):61-64 REISS AL; CIANCHETTI C; COHEN IL; DEVRIES B; HAGERMAN R; HINTON V; FROSTER U; LACHIEWICZ A; MAZZOCCO M; SOBESKY W; SUDHALTER V BRIEF SCREENING QUESTIONNAIRE FOR DETERMINING AFFECTED STATE IN FRAGILE-X SYNDROME - A CONSENSUS RECOMMENDATION | 2 | 3 |
| 562 | 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 |
| 563 | 11 | 18 | 913 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):72-77 LACHIEWICZ AM ABNORMAL BEHAVIORS OF YOUNG GIRLS WITH FRAGILE-X SYNDROME | 20 | 27 |
| 564 | 1 | 14 | 914 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):78-86 MAZZOCCO MMM; HAGERMAN RJ; PENNINGTON BF PROBLEM-SOLVING LIMITATIONS AMONG CYTOGENETICALLY EXPRESSING FRAGILE-X WOMEN | 23 | 31 |
| 565 | 15 | 23 | 915 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):87-95 HINTON VJ; DOBKIN CS; HALPERIN JM; JENKINS EC; BROWN WT; DING XH; COHEN IL; ROUSSEAU F; MIEZEJESKI CM MODE OF INHERITANCE INFLUENCES BEHAVIORAL EXPRESSION AND MOLECULAR CONTROL OF COGNITIVE DEFICITS IN FEMALE CARRIERS OF THE FRAGILE-X SYNDROME | 5 | 8 |
| 566 | 5 | 11 | 916 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):96-102 BROWN WT; JENKINS EC; GOONEWARDENA P; MIEZEJESKI C; ATKIN J; DEVYS D PRENATALLY DETECTED FRAGILE-X FEMALES - LONG-TERM FOLLOW-UP-STUDIES SHOW HIGH-RISK OF MENTAL IMPAIRMENT | 4 | 4 |
| 567 | 11 | 29 | 917 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):111-115 GRIGSBY J; KEMPER MB; HAGERMAN RJ VERBAL-LEARNING AND MEMORY AMONG HETEROZYGOUS FRAGILE-X FEMALES | 7 | 7 |
| 568 | 0 | 3 | 918 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):116-119 STEYAERT J; BORGHGRAEF M; GAULTHIER C; FRYNS JP; VANDENBERGHE H COGNITIVE PROFILE IN ADULT, NORMAL INTELLIGENT FEMALE FRAGILE-X CARRIERS | 6 | 9 |
| 569 | 6 | 10 | 919 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):120-123 PARTINGTON MW; ROBINSON H; LAING S; TURNER G MORTALITY IN THE FRAGILE-X SYNDROME - PRELIMINARY DATA | 2 | 3 |
| 570 | 1 | 16 | 920 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):124-127 TIROSH E; BOROCHOWITZ Z SLEEP-APNEA IN FRAGILE-X SYNDROME | 3 | 5 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 571 | 10 | 14 | 921 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):136-141 JENKINS EC; GENOVESE MJ; DUNCAN CJ; GU H; STARKHOUCK SL; LELE K; LI SY; KRAWCZUN MS FRA(X)(Q27.2), THE COMMON FRAGILE SITE, OBSERVED IN ONLY ONE OF 760 CASES STUDIED FOR THE FRAGILE-X SYNDROME | 1 | 1 |
| 572 | 11 | 21 | 922 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):142-148 FISCH GS; FRYNS JP FACTORS WHICH CONTRIBUTE TO CYTOGENETIC FREQUENCY OF EXPRESSION IN FAMILIES OF FRAGILE-X FEMALES | 1 | 1 |
| 573 | 12 | 19 | 923 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):155-160 JENKINS EC; DUNCAN CJ; GU H; GENOVESE M; KRAWCZUN MS DIALYZED FETAL BOVINE SERUM INCREASES CYTOGENETIC FRAGILE-X EXPRESSION | 1 | 1 |
| 574 | 2 | 5 | 924 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):161-161 HOWARDPEEBLES PN EFFECT OF DIALYZED SERA ON FRAGILE-X EXPRESSION | 0 | 0 |
| 575 | 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 |
| 576 | 7 | 9 | 926 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):167-169 SHAPIRO LR; WILMOT PL; ANDREE LE PRENATAL CYTOGENETIC DIAGNOSIS OF THE FRAGILE-X CHROMOSOME - FEASIBILITY AND SPEED OF INSITU CLONAL METHOD IN AMNIOTIC-FLUID CELL TISSUE-CULTURE | 0 | 0 |
| 577 | 4 | 6 | 927 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):170-173 SHAPIRO LR; WILMOT PL; FISCH GS PRENATAL CYTOGENETIC DIAGNOSIS OF THE FRAGILE-X SYNDROME IN AMNIOTIC-FLUID - CALCULATION OF ACCURACY | 1 | 1 |
| 578 | 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 |
| 579 | 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 |
| 580 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 581 | 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 |
| 582 | 16 | 19 | 932 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):197-207 ROUSSEAU F; HEITZ D; BIANCALANA V; OBERLE I; MANDEL JL ON SOME TECHNICAL ASPECTS OF DIRECT DNA DIAGNOSIS OF THE FRAGILE-X SYNDROME | 27 | 46 |
| 583 | 10 | 15 | 933 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):208-216 DEVYS D; BIANCALANA V; ROUSSEAU F; BOUE J; MANDEL JL; OBERLE I ANALYSIS OF FULL FRAGILE-X MUTATIONS IN FETAL TISSUES AND MONOZYGOTIC TWINS INDICATE THAT ABNORMAL METHYLATION AND SOMATIC HETEROGENEITY ARE ESTABLISHED EARLY IN DEVELOPMENT | 58 | 89 |
| 584 | 13 | 21 | 934 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):217-223 KNIGHT SJL; HIRST MC; ROCHE A; CHRISTODOULOU Z; HUSON SM; WINTER R; FITCHETT M; MCKINLEY MJ; LINDENBAUM RH; NAKAHORI Y; DAVIES KE MOLECULAR STUDIES OF THE FRAGILE-X SYNDROME | 10 | 19 |
| 585 | 14 | 25 | 935 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):237-243 RIGGINS GJ; SHERMAN SL; OOSTRA BA; SUTCLIFFE JS; FEITELL D; NELSON DL; VANOOST BA; SMITS APT; RAMOS FJ; PFENDNER E; KUHL DPA; CASKEY CT; WARREN ST CHARACTERIZATION OF A HIGHLY POLYMORPHIC DINUCLEOTIDE REPEAT 150-KB PROXIMAL TO THE FRAGILE-X SITE | 35 | 57 |
| 586 | 13 | 22 | 936 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):244-254 SNOW K; DOUD L; HAGERMAN R; HULL C; HIRST MC; DAVIES KE; THIBODEAU SL ANALYSIS OF MUTATIONS AT THE FRAGILE-X LOCUS USING THE DNA PROBE OX1.9 | 14 | 16 |
| 587 | 15 | 17 | 937 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):268-278 MALMGREN H; STEENBONDESON ML; GUSTAVSON KH; SEEMANOVA E; HOLMGREN G; OBERLE I; MANDEL JL; PETTERSSON U; DAHL N METHYLATION AND MUTATION PATTERNS IN THE FRAGILE-X SYNDROME | 13 | 17 |
| 588 | 12 | 15 | 938 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):282-290 TEJADA I; MORNET E; BIANCALANA V; OBERLE I; BOUE J; MANDEL JL; BOUE A DIRECT DNA ANALYSIS OF FRAGILE-X SYNDROME IN SPANISH PEDIGREES | 7 | 7 |
| 589 | 14 | 40 | 939 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):291-298 MIGEON BR CONCERNING THE ROLE OF X-INACTIVATION AND DNA METHYLATION IN FRAGILE X-SYNDROME | 3 | 4 |
| 590 | 25 | 46 | 940 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):299-306 CLARKE A; BRADLEY D; GILLESPIE K; REES D; HOLLAND A; THOMAS NST FRAGILE-X MENTAL-RETARDATION AND THE IDURONATE SULFATASE LOCUS - TESTING LAIRD MODEL OF FRA(X) INHERITANCE | 7 | 12 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 591 | 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 |
| 592 | 7 | 22 | 942 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):312-319 CARPENTER NJ; SWARTZBOYD J; PRICHARD JK; LAM T LINKAGE AND RISK ASSESSMENT IN FRAGILE-X FAMILIES USING NEW DNA PROBES AT XQ27 | 1 | 1 |
| 593 | 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 |
| 594 | 4 | 6 | 944 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):328-332 NOLIN SL; SNIDER DA; JENKINS EC; DOBKIN CS; PATCHELL K; KRAWCZUN M; STRONG G; COLWELL M; VICTOR A; PAYYAPILLI T; TURCZYN M; LITTLE A; NAGARAJA U; DOYLE N; KENEFICK B; SULLIVAN C NEW-YORK-STATE SCREENING-PROGRAM FOR FRAGILE-X SYNDROME - A PROGRESS REPORT | 7 | 8 |
| 595 | 16 | 19 | 945 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):333-338 GABARRON J; LOPEZ I; GLOVER G; CARBONELL P FRAGILE-X SCREENING-PROGRAM IN A SPANISH REGION | 8 | 10 |
| 596 | 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 |
| 597 | 3 | 3 | 947 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):353-354 DRUGGE U; HOLMGREN G; SONBLOMQUIST HK; DAHL N; GUSTAVSON KH; MALMGREN H STUDY OF INDIVIDUALS POSSIBLY AFFECTED WITH THE FRAGILE-X SYNDROME IN A LARGE SWEDISH FAMILY IN THE 18TH TO 20TH CENTURIES | 7 | 7 |
| 598 | 6 | 8 | 948 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):355-360 SHERMAN SL; BARBI G; BRONDUMNIELSEN K; BROWN WT; CARPENTER NJ; CHUDLEY AE; FERRAZ OP; FERREIRA P; GUSTAVSON KH; HALLIDAY J; HOCKEY A; HOWARDPEEBLES PN; JENKINS E; KENNERKNECHT I; KAHKONEN M; LADAIQUE P; LEISTI J; MADDALENA A; MAZURCZAK T; MATTEI JF; MATTINA T; MCKINLEY MJ; MURPHY P; PELLISSIER MC; PURVISSMITH S; ROBINSON H; SCAPAGNINI U; SCHAAP T; SHAPIRO LR; SMITS APT; STEINBACH P; TURNER G; UCHIDA IA; VANOOST BA; VOELCKEL MA; WEAVER DD; WEBB T COLLABORATIVE PROSPECTIVE-STUDY OF THE FRAGILE-X SYNDROME - ONE-YEAR PROGRESS REPORT | 2 | 4 |
| 599 | 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 |
| 600 | 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 |
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