| Missing Links? Citation Matrix | Graphs | Glossary HistCite Guide About |
Nodes: 2647,
Authors: 5321,
Journals: 428,
Outer References: 16458,
Words: 3536
Collection span: 1967 - 2005
View: Overview. Sorted by year, source, volume, issue, page.
Page 3: 1 2 3 4 5 6 7 8 9
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 601 | 0 | 0 | 601 1988 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 18(3):458-458 SCHOPLER E ON THE ASSOCIATION OF FRAGILE-X WITH AUTISM - RESPONSE | 0 | 0 |
| 602 | 2 | 6 | 602 1988 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 18(3):458-460 LECOUTEUR A; RUTTER M; SUMMERS D; BUTLER L FRAGILE-X IN FEMALE AUTISTIC TWINS | 8 | 14 |
| 603 | 1 | 11 | 603 1988 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 18(4):681-685 TSAI LY; CROWE RR; PATIL SR; MURRAY J; QUINN J SEARCH FOR DNA MARKERS IN 2 AUTISTIC MALES WITH THE FRAGILE-X SYNDROME | 2 | 3 |
| 604 | 3 | 13 | 604 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 |
| 605 | 1 | 1 | 605 1988 JOURNAL OF MEDICAL GENETICS 25(1):64-64 LACA Z; BRANKOVIC S EXPRESSION OF FRAGILE X-CHROMOSOME AND POSSIBLE DELETION IN SUCCESSIVE CELL DIVISIONS | 0 | 0 |
| 606 | 0 | 0 | 606 1988 JOURNAL OF MEDICAL GENETICS 25(2):128-128 ENGLISH C ANTHROPOMETRIC STUDIES IN THE FRAGILE X-SYNDROME | 0 | 0 |
| 607 | 0 | 0 | 607 1988 JOURNAL OF MEDICAL GENETICS 25(2):129-129 DAVIES KE; PATTERSON M; BELL M; KENWRICK SJ MOLECULAR ANALYSIS OF THE FRAGILE X-SYNDROME | 0 | 0 |
| 608 | 0 | 0 | 608 1988 JOURNAL OF MEDICAL GENETICS 25(2):131-131 MCKINLEY MJ; KEARNEY LU; NICOLAIDES K PRENATAL-DIAGNOSIS OF FRAGILE X-SYNDROME BY PLACENTAL BIOPSY | 0 | 0 |
| 609 | 5 | 17 | 609 1988 JOURNAL OF MEDICAL GENETICS 25(6):407-414 LOESCH DZ; HAY DA CLINICAL-FEATURES AND REPRODUCTIVE PATTERNS IN FRAGILE-X FEMALE HETEROZYGOTES | 33 | 43 |
| 610 | 0 | 0 | 610 1988 NEUROTOXICOLOGY 9(1):139-140 EDWARDS DR; KEPPEN LD; GOLLIN SM AUTISM AND FRAGILE-X SYNDROME | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 611 | 5 | 9 | 611 1988 NEUROTOXICOLOGY 9(3):359-365 EDWARDS DR; KEPPEN LD; RANELLS JD; GOLLIN SM AUTISM IN ASSOCIATION WITH FRAGILE X-SYNDROME IN FEMALES - IMPLICATIONS FOR DIAGNOSIS AND TREATMENT IN CHILDREN | 4 | 7 |
| 612 | 27 | 63 | 612 1988 QUARTERLY JOURNAL OF MEDICINE 69(258):755-763 FROSTERISKENIUS U; PATTERSON MN; BELL MV; BLOOMFIELD J; DAVIES KE MOLECULAR ANALYSIS OF THE FRAGILE-X SYNDROME | 1 | 1 |
| 613 | 3 | 31 | 613 1988 SCHIZOPHRENIA RESEARCH 1(4):277-281 DELISI LE; REISS AL; WHITE BJ; GERSHON ES CYTOGENETIC STUDIES OF MALES WITH SCHIZOPHRENIA - SCREENING FOR THE FRAGILE X-CHROMOSOME AND OTHER CHROMOSOMAL-ABNORMALITIES | 1 | 36 |
| 614 | 0 | 0 | 614 1988 ZEITSCHRIFT FUR KLINISCHE MEDIZIN-ZKM 43(6):451-454 STEINBICKER V; SEEMANOVA E; MISSBACH D THE SYNDROME OF THE FRAGILE X (MARTIN-BELL-SYNDROME MBS) | 0 | 1 |
| 615 | 0 | 0 | 615 1989 AMERICAN FAMILY PHYSICIAN 39(5):185-193 SIMENSEN RJ; ROGERS RC FRAGILE-X SYNDROME | 1 | 1 |
| 616 | 14 | 29 | 616 1989 AMERICAN JOURNAL OF HUMAN GENETICS 45(2):304-309 DAHL N; GOONEWARDENA P; MALMGREN H; GUSTAVSON KH; HOLMGREN G; et al. LINKAGE ANALYSIS OF FAMILIES WITH FRAGILE-X MENTAL-RETARDATION, USING A NOVEL RFLP MARKER (DXS 304) | 19 | 40 |
| 617 | 9 | 24 | 617 1989 AMERICAN JOURNAL OF HUMAN GENETICS 45(5):697-705 REISS AL; FREUND L; VINOGRADOV S; HAGERMAN R; CRONISTER A PARENTAL INHERITANCE AND PSYCHOLOGICAL DISABILITY IN FRAGILE-X FEMALES | 26 | 31 |
| 618 | 4 | 10 | 618 1989 AMERICAN JOURNAL OF HUMAN GENETICS 45(6):977-978 FERRI R BRAIN-STEM AUDITORY EVOKED-POTENTIALS IN THE FRAGILE-X SYNDROME | 2 | 3 |
| 619 | 2 | 7 | 619 1989 AMERICAN JOURNAL OF HUMAN GENETICS 45(6):978-979 ARINAMI T BRAIN-STEM AUDITORY EVOKED-POTENTIALS IN THE FRAGILE-X SYNDROME - REPLY | 0 | 0 |
| 620 | 7 | 18 | 620 1989 AMERICAN JOURNAL OF MEDICAL GENETICS 33(1):92-99 BRIDGE PJ; LILLICRAP DP MOLECULAR DIAGNOSIS OF THE FRAGILE-X [FRA-(X)] SYNDROME - CALCULATION OF RISKS BASED ON FLANKING DNA MARKERS IN SMALL PHASE-UNKNOWN FAMILIES | 0 | 4 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 621 | 5 | 19 | 621 1989 AMERICAN JOURNAL OF MEDICAL GENETICS 33(2):200-208 LOESCH DZ; WILSON SR MULTIVARIATE-ANALYSIS OF BODY SHAPE IN FRAGILE-X (MARTIN-BELL) SYNDROME | 2 | 5 |
| 622 | 11 | 30 | 622 1989 AMERICAN JOURNAL OF MEDICAL GENETICS 33(4):513-518 HAGERMAN RJ; SCHREINER RA; KEMPER MB; WITTENBERGER MD; ZAHN B; et al. LONGITUDINAL IQ CHANGES IN FRAGILE-X MALES | 37 | 49 |
| 623 | 21 | 44 | 623 1989 AMERICAN JOURNAL OF MEDICAL GENETICS 34(2):187-193 EINFELD S; MOLONY H; HALL W AUTISM IS NOT ASSOCIATED WITH THE FRAGILE-X SYNDROME | 31 | 53 |
| 624 | 10 | 14 | 624 1989 AMERICAN JOURNAL OF MEDICAL GENETICS 34(2):302-303 COHEN IL; BROWN WT; JENKINS EC; KRAWCZUN MS; FRENCH JH; et al. FRAGILE-X SYNDROME IN FEMALES WITH AUTISM | 13 | 16 |
| 625 | 30 | 58 | 625 1989 AMERICAN JOURNAL OF ORTHOPSYCHIATRY 59(1):142-152 HAGERMAN RJ; SOBESKY WE PSYCHOPATHOLOGY IN FRAGILE-X-SYNDROME | 29 | 41 |
| 626 | 0 | 0 | 626 1989 AMERICAN JOURNAL OF PHYSICAL ANTHROPOLOGY 78(2):200-200 BUTLER MG; HAYNES JL; ALLEN GA; SINGH DN ANTHROPOMETRIC COMPARISON OF MENTALLY-RETARDED MALES WITH AND WITHOUT FRAGILE X-SYNDROME | 0 | 0 |
| 627 | 11 | 24 | 627 1989 AMERICAN JOURNAL ON MENTAL RETARDATION 93(4):406-411 WOLFF PH; GARDNER J; PACCIA J; LAPPEN J THE GREETING BEHAVIOR OF FRAGILE X-MALES | 26 | 39 |
| 628 | 4 | 53 | 628 1989 AMERICAN ZOOLOGIST 29(2):569-591 LAIRD CD FROM POLYTENE CHROMOSOMES TO HUMAN EMBRYOLOGY - CONNECTIONS VIA THE HUMAN FRAGILE-X SYNDROME | 1 | 3 |
| 629 | 38 | 83 | 629 1989 ARCHIVES FRANCAISES DE PEDIATRIE 46(3):211-216 LELOUARN P; MORAINE C; PERROT A; BARTHELEMY C; GARREAU B; et al. AUTISM AND FRAGILE X-SYNDROME | 3 | 5 |
| 630 | 6 | 8 | 630 1989 ARCHIVES OF DISEASE IN CHILDHOOD 64(9):1223-1224 WINTER RM FRAGILE-X MENTAL-RETARDATION | 1 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 631 | 2 | 17 | 631 1989 ARCHIVES OF NEUROLOGY 46(12):1269-1270 GRIGSBY J; HAGERMAN R FRAGILE-X SYNDROME - A GENETIC ETIOLOGY FOR DEVELOPMENTAL GERSTMANN SYNDROME | 0 | 0 |
| 632 | 0 | 29 | 632 1989 BLOOD 74(2):828-832 MORLE L; MORLE F; ROUX AF; GODET J; FORGET BG; et al. SPECTRIN TUNIS (SP-ALPHA-I/78), AN ELLIPTOCYTOGENIC VARIANT, IS DUE TO THE CGG -] TGG CODON CHANGE (ARG -] TRP) AT POSITION-35 OF THE ALPHA-I DOMAIN | 0 | 33 |
| 633 | 4 | 9 | 633 1989 BRITISH HEART JOURNAL 61(3):289-291 SREERAM N; WREN C; BHATE M; ROBERTSON P; HUNTER S CARDIAC ABNORMALITIES IN THE FRAGILE X-SYNDROME | 6 | 9 |
| 634 | 2 | 31 | 634 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 |
| 635 | 9 | 14 | 635 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 |
| 636 | 0 | 0 | 636 1989 CLINICAL RESEARCH 37(1):A170-A170 HAGERMAN RJ; SCHREINER RA; KEMPER MB; WITTENBERGER MD; ZAHN B; et al. LONGITUDINAL IQ CHANGES IN FRAGILE-X MALES | 0 | 0 |
| 637 | 2 | 10 | 637 1989 CYTOGENETICS AND CELL GENETICS 50(2-3):172-173 SAUER SM; PHELAN MC; RICHER CL; SCHWARTZ CE PHYSICAL MAPPING OF PROBES PROXIMAL TO THE FRAGILE-X LOCUS (FRAX) CONFIRMS THE ORDER F9-DXS105 (CX55.7)-DXS98 (4D8)-FRAXA | 1 | 1 |
| 638 | 0 | 0 | 638 1989 CYTOGENETICS AND CELL GENETICS 51(1-4):982-982 DAHL N; MALMSTROM H; HAMMARSTROMHEEROMA K; WADELIUS C; GUSTAVSON KH; et al. ISOLATION OF A NEW DNA MARKER TIGHTLY LINKED TO THE FRAGILE-X LOCUS (FRAXA) | 0 | 3 |
| 639 | 0 | 0 | 639 1989 CYTOGENETICS AND CELL GENETICS 51(1-4):1007-1007 GOONEWARDENA P; GROSS AC; FERRANDO CJ; BROWN T; DAHL N; et al. ANONYMOUS DNA PROBE U6.2 (DXS304) FROM XQ MAPS DISTAL TO THE DXS98 LOCUS AND SHOWS CLOSE LINKAGE TO THE FRAGILE-X SYNDROME | 0 | 1 |
| 640 | 0 | 0 | 640 1989 CYTOGENETICS AND CELL GENETICS 51(1-4):1009-1009 GROSS AC; FERRANDO CJ; BROWN WT LINKAGE DATA FOR FRAGILE-X AND 3 DISTAL MARKERS | 0 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 641 | 0 | 0 | 641 1989 CYTOGENETICS AND CELL GENETICS 51(1-4):1086-1087 SUTHERLAND GR; BAKER E THE COMMON FRAGILE SITE (FRAXD) IS AT XQ27.2 AND CAN BE DISTINGUISHED FROM THE FRAGILE-X (FRAXA) AT XQ27.3 | 2 | 8 |
| 642 | 0 | 0 | 642 1989 CYTOGENETICS AND CELL GENETICS 51(1-4):1089-1090 THIBODEAU SN; SCHAID D; BREN G; BLOOMFIELD J; BELL MV; et al. GENETIC-MAPPING OF A NOVEL REGION CLOSE TO THE FRAGILE X-SITE ON THE HUMAN X-CHROMOSOME | 0 | 1 |
| 643 | 0 | 1 | 643 1989 CYTOGENETICS AND CELL GENETICS 51(1-4):1100-1101 WAHLSTROM J; WITTENGERSTROM I; ANVRET M; ODEN A; JOHANNESSON T; et al. RETT SYNDROME RELATED TO FRAGILE X(P22) IN CAFFEINE-INDUCED LYMPHOCYTES CULTURES | 0 | 2 |
| 644 | 0 | 0 | 644 1989 GENOMICS 4(4):570-578 PATTERSON MN; BELL MV; BLOOMFIELD J; FLINT T; DORKINS H; et al. GENETIC AND PHYSICAL MAPPING OF A NOVEL REGION CLOSE TO THE FRAGILE X-SITE ON THE HUMAN X-CHROMOSOME | 17 | 43 |
| 645 | 0 | 0 | 645 1989 GENOMICS 5(4):797-801 VINCENT A; DAHL N; OBERLE I; HANAUER A; MANDEL JL; et al. THE POLYMORPHIC MARKER DXS304 IS WITHIN 5-CENTIMORGANS OF THE FRAGILE-X LOCUS | 13 | 23 |
| 646 | 4 | 22 | 646 1989 HUMAN GENETICS 81(4):377-381 TOMMERUP N INDUCTION OF THE FRAGILE X ON BRDU-SUBSTITUTED CHROMOSOMES WITH DIRECT VISUALIZATION OF SISTER CHROMATID EXCHANGES ON BANDED CHROMOSOMES | 4 | 4 |
| 647 | 10 | 17 | 647 1989 HUMAN GENETICS 82(1):79-81 SCHAAP T THE ROLE OF RECOMBINATION IN THE EVOLVEMENT OF THE FRAGILE X-MUTATION | 2 | 2 |
| 648 | 7 | 16 | 648 1989 HUMAN GENETICS 82(3):216-218 DAHL N; HAMMARSTROMHEEROMA K; GOONEWARDENA P; WADELIUS C; GUSTAVSON KH; et al. ISOLATION OF A DNA PROBE OF POTENTIAL USE FOR DIAGNOSIS OF THE FRAGILE-X SYNDROME | 17 | 32 |
| 649 | 9 | 19 | 649 1989 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 19(2):343-347 HO HH; KALOUSEK DK BRIEF REPORT - FRAGILE X-SYNDROME IN AUTISTIC BOYS | 10 | 14 |
| 650 | 6 | 7 | 650 1989 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 19(3):473-476 BOLTON P; RUTTER M; BUTLER L; SUMMERS D FEMALES WITH AUTISM AND THE FRAGILE-X | 7 | 11 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 651 | 0 | 1 | 651 1989 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 19(4):643-643 LACHIEWICZ AM FRAGILE-X SYNDROME - A HANDBOOK FOR FAMILIES AND EDUCATORS - FINUCANE,B | 0 | 0 |
| 652 | 2 | 33 | 652 1989 JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY AND ALLIED DISCIPLINES 30(6):845-856 COHEN IL; VIETZE PM; SUDHALTER V; JENKINS EC; BROWN WT PARENT CHILD DYADIC GAZE PATTERNS IN FRAGILE-X MALES AND IN NON-FRAGILE-X MALES WITH AUTISTIC DISORDER | 31 | 49 |
| 653 | 4 | 9 | 653 1989 JOURNAL OF MEDICAL GENETICS 26(7):439-442 VOULLAIRE LE; WEBB GC; LEVERSHA M FRAGILE X-TESTING IN A DIAGNOSTIC CYTOGENETICS LABORATORY | 3 | 7 |
| 654 | 10 | 16 | 654 1989 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 28(3):417-421 PAYTON JB; STEELE MW; WENGER SL; MINSHEW NJ THE FRAGILE-X MARKER AND AUTISM IN PERSPECTIVE | 19 | 37 |
| 655 | 5 | 34 | 655 1989 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 28(3):422-426 DYKENS EM; HODAPP RM; ORT S; FINUCANE B; SHAPIRO LR; et al. THE TRAJECTORY OF DEVELOPMENT IN MALES WITH FRAGILE-X SYNDROME | 33 | 52 |
| 656 | 9 | 27 | 656 1989 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 28(3):427-430 DYKENS EM; HODAPP RM; LECKMAN JF ADAPTIVE AND MALADAPTIVE FUNCTIONING OF INSTITUTIONALIZED AND NONINSTITUTIONALIZED FRAGILE-X MALES | 17 | 28 |
| 657 | 4 | 4 | 657 1989 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 28(6):965-966 FISCH GS FRAGILE-X AND AUTISM | 3 | 4 |
| 658 | 3 | 4 | 658 1989 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 28(6):966-966 PAYTON JB; STEELE MW; WENGER SL; MINSHEW NJ FRAGILE-X AND AUTISM | 2 | 2 |
| 659 | 1 | 5 | 659 1989 LANCET 2(8657):279-279 SCHEPIS C; PALAZZO R; RAGUSA RM; SPINA E; BARLETTA C ASSOCIATION OF CUTIS VERTICIS GYRATA WITH FRAGILE-X SYNDROME AND FRAGILITY OF CHROMOSOME-12 | 0 | 11 |
| 660 | 0 | 0 | 660 1989 M S-MEDECINE SCIENCES 5(7):450-458 JORDAN BR; MATTEI JF FRAGILE X-LINKED MENTAL-RETARDATION, 1989 | 2 | 2 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 661 | 0 | 1 | 661 1989 NATURE 341(6243):580-580 HARRIS A; BOBROW M THE FRAGILE-X SYNDROME - DAVIES,KE | 0 | 0 |
| 662 | 0 | 0 | 662 1989 NEUROLOGIC CLINICS 7(1):107-121 BROWN WT THE FRAGILE-X SYNDROME | 1 | 1 |
| 663 | 0 | 4 | 663 1989 NUCLEIC ACIDS RESEARCH 17(24):10513-10513 GRUNDY C; CHITOLIE A; TALBOT S; BEVAN D; KAKKAR V; et al. PROTEIN-C LONDON .1. RECURRENT MUTATION AT ARG-169 (CGG-]TGG) IN THE PROTEIN-C GENE CAUSING THROMBOSIS | 0 | 19 |
| 664 | 0 | 0 | 664 1989 PEDIATRIC RESEARCH 25(4):A16-A16 MERYASH DL PERCEPTION OF BURDEN AMONG AT-RISK WOMEN OF RAISING A CHILD WITH FRAGILE-X SYNDROME | 0 | 0 |
| 665 | 8 | 19 | 665 1989 PEDIATRICS 83(4):547-552 SIMKO A; HORNSTEIN L; SOUKUP S; BAGAMERY N FRAGILE X-SYNDROME - RECOGNITION IN YOUNG-CHILDREN | 28 | 31 |
| 666 | 3 | 3 | 666 1989 PRENATAL DIAGNOSIS 9(11):777-781 WEBB TP; BUNDEY S; MCKINLEY M MISSED PRENATAL-DIAGNOSIS OF FRAGILE-X SYNDROME | 3 | 5 |
| 667 | 21 | 41 | 667 1989 PSYCHOLOGY IN THE SCHOOLS 26(4):380-389 SIMENSEN RJ; ROGERS RC SCHOOL-PSYCHOLOGY AND MEDICAL DIAGNOSIS - THE FRAGILE X-SYNDROME | 1 | 1 |
| 668 | 0 | 0 | 668 1989 REVISTA BRASILEIRA DE GENETICA 12(2):391-404 NAVAJAS L; VIANNAMORGANTE AM RELATIONSHIP BETWEEN AGE AND MENTAL STATUS AND THE EXPRESSION OF THE FRAGILE(X) IN HETEROZYGOTES FOR THE MARTIN-BELL SYNDROME | 0 | 0 |
| 669 | 0 | 3 | 669 1989 SCIENCE 243(4888):171-172 BARNES DM FRAGILE-X SYNDROME AND ITS PUZZLING GENETICS | 3 | 9 |
| 670 | 4 | 22 | 670 1989 SCIENCE 246(4935):1298-1300 SUTHERS GK; CALLEN DF; HYLAND VJ; KOZMAN HM; BAKER E; et al. A NEW DNA MARKER TIGHTLY LINKED TO THE FRAGILE-X LOCUS (FRAXA) | 31 | 66 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 671 | 2 | 3 | 671 1989 ZEITSCHRIFT FUR KINDER-UND JUGENDPSYCHIATRIE UND PSYCHOTHERAPIE 17(2):85-90 BLANK R MAIN SYMPTOMS - DELAYED LANGUAGE-DEVELOPMENT AND BEHAVIOR PROBLEMS - 2 CASE-REPORTS ON THE FRAGILE-X SYNDROME | 1 | 1 |
| 672 | 30 | 39 | 672 1989 ZEITSCHRIFT FUR KINDER-UND JUGENDPSYCHIATRIE UND PSYCHOTHERAPIE 17(2):91-97 VONGONTARD A PSYCHOPATHOLOGY ASSOCIATED WITH THE FRAGILE-X SYNDROME | 1 | 2 |
| 673 | 0 | 0 | 673 1989 ZHURNAL NEVROPATOLOGII I PSIKHIATRII IMENI S S KORSAKOVA 89(8):101-105 BLYUMINA MG CLINICAL SIGNS OF OLIGOPHRENIA WITH FRAGILE X-CHROMOSOME IN PREPUBERTY AND POSTPUBERTY MALES | 1 | 2 |
| 674 | 5 | 14 | 674 1990 AMERICAN JOURNAL OF HUMAN GENETICS 46(3):443-451 SVED JA; LAIRD CD POPULATION GENETIC CONSEQUENCES OF THE FRAGILE-X SYNDROME, BASED ON THE X-INACTIVATION IMPRINTING MODEL | 12 | 22 |
| 675 | 19 | 66 | 675 1990 AMERICAN JOURNAL OF HUMAN GENETICS 46(4):696-719 LAIRD CD; LAMB MM; THORNE JL 2 PROGENITOR CELLS FOR HUMAN OOGONIA INFERRED FROM PEDIGREE DATA AND THE X-INACTIVATION IMPRINTING MODEL OF THE FRAGILE-X SYNDROME | 28 | 34 |
| 676 | 12 | 33 | 676 1990 AMERICAN JOURNAL OF HUMAN GENETICS 46(4):738-743 ROCCHI M; ARCHIDIACONO N; RINALDI A; FILIPPI G; BARTOLUCCI G; et al. MENTAL-RETARDATION IN HETEROZYGOTES FOR THE FRAGILE-X MUTATION - EVIDENCE IN FAVOR OF AN X INACTIVATION-DEPENDENT EFFECT | 11 | 13 |
| 677 | 11 | 44 | 677 1990 AMERICAN JOURNAL OF HUMAN GENETICS 46(4):744-753 KHALIFA MM; REISS AL; MIGEON BR METHYLATION STATUS OF GENES FLANKING THE FRAGILE SITE IN MALES WITH THE FRAGILE-X SYNDROME - A TEST OF THE IMPRINTING HYPOTHESIS | 4 | 7 |
| 678 | 18 | 37 | 678 1990 AMERICAN JOURNAL OF HUMAN GENETICS 47(2):175-180 BROWN WT INVITED EDITORIAL - THE FRAGILE-X - PROGRESS TOWARD SOLVING THE PUZZLE | 29 | 41 |
| 679 | 6 | 24 | 679 1990 AMERICAN JOURNAL OF HUMAN GENETICS 47(2):181-187 MACKINNON RN; HIRST MC; BELL MV; WATSON JEV; CLAUSSEN U; et al. MICRODISSECTION OF THE FRAGILE-X REGION | 9 | 37 |
| 680 | 6 | 38 | 680 1990 AMERICAN JOURNAL OF HUMAN GENETICS 47(2):187-195 SUTHERS GK; HYLAND VJ; CALLEN DF; OBERLE I; ROCCHI M; et al. PHYSICAL MAPPING OF NEW DNA PROBES NEAR THE FRAGILE-X MUTATION (FRAXA) BY USING A PANEL OF CELL-LINES | 26 | 64 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 681 | 19 | 35 | 681 1990 AMERICAN JOURNAL OF HUMAN GENETICS 47(3):395-402 SOOD R; MULLIGAN LM; POON R; WHITE BN; HOLDEN JJA GENETIC-MAPPING OF 2 NEW DNA MARKERS IN XQ26-Q28 RELATIVE TO THE FRAGILE-X SYNDROME LOCUS | 3 | 7 |
| 682 | 12 | 20 | 682 1990 AMERICAN JOURNAL OF HUMAN GENETICS 47(6):988-993 OHASHI H; KUWANO A; TSUKAHARA M; ARINAMI T; KAJII T REPLICATION PATTERNS OF THE FRAGILE-X IN HETEROZYGOUS CARRIERS - ANALYSIS BY A BRDURD ANTIBODY METHOD | 1 | 2 |
| 683 | 19 | 43 | 683 1990 AMERICAN JOURNAL OF MEDICAL GENETICS 35(1):22-27 MINGRONINETTO RC; ROSENBERG C; VIANNAMORGANTE AM; PAVANELLO RDM FRAGILE-X FREQUENCY IN A MENTALLY-RETARDED POPULATION IN BRAZIL | 5 | 8 |
| 684 | 7 | 30 | 684 1990 AMERICAN JOURNAL OF MEDICAL GENETICS 35(1):28-35 GRIGSBY JP; KEMPER MB; HAGERMAN RJ; MYERS CS NEUROPSYCHOLOGICAL DYSFUNCTION AMONG AFFECTED HETEROZYGOUS FRAGILE-X FEMALES | 24 | 29 |
| 685 | 9 | 16 | 685 1990 AMERICAN JOURNAL OF MEDICAL GENETICS 36(1):122-125 VANROY BC; WILLEMS PJ; VITS LJ; CEULEMANS BP; COUCKE PJ; et al. 2 BROTHERS WITH MENTAL-RETARDATION DISCORDANT FOR THE FRAGILE-X SYNDROME | 4 | 4 |
| 686 | 6 | 17 | 686 1990 AMERICAN JOURNAL OF MEDICAL GENETICS 37(2):265-267 MOORE PSJ; CHUDLEY AE; WINTER JSD TRUE PRECOCIOUS PUBERTY IN A GIRL WITH THE FRAGILE X-SYNDROME | 10 | 13 |
| 687 | 1 | 2 | 687 1990 AMERICAN JOURNAL OF MEDICAL GENETICS 37(3):433-433 MEISNER LF FRAGILE-X FREQUENCY | 0 | 0 |
| 688 | 1 | 1 | 688 1990 AMERICAN JOURNAL OF MEDICAL GENETICS 37(3):434-434 MINGRONINETTO RC; ROSENBERG C; VIANNAMORGANTE AM; PAVANELLO RCM FRAGILE-X FREQUENCY - RESPONSE | 0 | 0 |
| 689 | 2 | 6 | 689 1990 AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY 163(5):1713-1714 SINDWANI V; VERMA RS CYTOGENETIC UNCERTAINTIES SURROUNDING THE FRAGILE X IN MARTIN-BELL SYNDROME | 0 | 0 |
| 690 | 11 | 23 | 690 1990 AMERICAN JOURNAL ON MENTAL RETARDATION 94(4):431-441 SUDHALTER V; COHEN IL; SILVERMAN W; WOLFSCHEIN EG CONVERSATIONAL ANALYSES OF MALES WITH FRAGILE-X, DOWN SYNDROME, AND AUTISM - COMPARISON OF THE EMERGENCE OF DEVIANT LANGUAGE | 56 | 70 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 691 | 9 | 32 | 691 1990 AMERICAN JOURNAL ON MENTAL RETARDATION 94(4):442-447 CANTU ES; STONE JW; WING AA; LANGEE HR; WILLIAMS CA CYTOGENETIC SURVEY FOR AUTISTIC FRAGILE-X CARRIERS IN A MENTAL-RETARDATION CENTER | 5 | 16 |
| 692 | 8 | 13 | 692 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 |
| 693 | 0 | 0 | 693 1990 ANNALS OF NEUROLOGY 28(3):440-440 BERRYKRAVIS E; HUTTENLOCHER PR CYCLIC-AMP METABOLISM IN FRAGILE X-SYNDROME | 0 | 0 |
| 694 | 1 | 40 | 694 1990 ARCHIVES FRANCAISES DE PEDIATRIE 47(10):701-703 PIUSSAN C X-LINKED MENTAL-RETARDATION WITHOUT FRAGILE X-CHROMOSOME | 0 | 0 |
| 695 | 2 | 4 | 695 1990 ARCHIVES OF DISEASE IN CHILDHOOD 65(3):335-335 REDINGTON A; BUSH A FRAGILE-X MENTAL-RETARDATION | 2 | 2 |
| 696 | 28 | 73 | 696 1990 BIOLOGICAL PSYCHIATRY 27(2):223-240 REISS AL; FREUND L FRAGILE X-SYNDROME | 22 | 28 |
| 697 | 1 | 14 | 697 1990 BRAIN & DEVELOPMENT 12(1):128-130 WAHLSTROM J; WITTENGERSTROM I; MELLQUIST L; ANVRET M; ODEN A THE RETT SYNDROME RELATED TO FRAGILE-X(P22) IN CAFFEINE-INDUCED LYMPHOCYTE CULTURE | 0 | 13 |
| 698 | 2 | 14 | 698 1990 BRITISH DENTAL JOURNAL 168(4):160-162 NUNN JH; DURNING P FRAGILE-X (MARTIN BELL) SYNDROME AND DENTAL-CARE | 0 | 0 |
| 699 | 6 | 13 | 699 1990 BRITISH JOURNAL OF HOSPITAL MEDICINE 43(1):17-17 BUNDEY S FRAGILE-X SYNDROME | 1 | 1 |
| 700 | 24 | 44 | 700 1990 CLINICAL GENETICS 37(1):2-11 SUTHERLAND GR; MULLEY JC DIAGNOSTIC MOLECULAR-GENETICS OF THE FRAGILE-X | 14 | 16 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 701 | 5 | 23 | 701 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 | 30 | 43 |
| 702 | 13 | 27 | 702 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 | 17 | 20 |
| 703 | 0 | 0 | 703 1990 CLINICAL RESEARCH 38(1):A164-A164 HAGERMAN R; AMIRI K; CRONISTER A; WITTENBERGER M; SCHREINER R; et al. FRAGILE-X GIRLS - PHYSICAL AND NEUROCOGNITIVE STATUS AND OUTCOME | 0 | 0 |
| 704 | 1 | 12 | 704 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 |
| 705 | 10 | 27 | 705 1990 EUROPEAN NEUROLOGY 30(1):32-37 RAIMONDI E; LENTI C; ROMAGNONI M; NEGRI R; GAMBINI E; et al. FRAGILE-X MENTAL-RETARDATION IN A LARGE 5-GENERATION FAMILY - A CLINICAL AND CYTOGENETIC STUDY | 0 | 0 |
| 706 | 6 | 12 | 706 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 |
| 707 | 5 | 14 | 707 1990 HUMAN GENETICS 84(3):263-266 ROUSSEAU F; VINCENT A; OBERLE I; MANDEL JL NEW INFORMATIVE POLYMORPHISM AT THE DXS304 LOCUS, A CLOSE DISTAL MARKER FOR THE FRAGILE X-LOCUS | 4 | 19 |
| 708 | 6 | 44 | 708 1990 HUMAN GENETICS 84(4):347-352 SCHMIDT M; CERTOMA A; DUSART D; KALITSIS P; LEVERSHA M; et al. UNUSUAL X-CHROMOSOME INACTIVATION IN A MENTALLY-RETARDED GIRL WITH AN INTERSTITIAL DELETION XQ27 - IMPLICATIONS FOR THE FRAGILE X-SYNDROME | 7 | 27 |
| 709 | 5 | 7 | 709 1990 HUMAN GENETICS 85(1):141-142 SUTHERS GK; SUTHERLAND GR RECOMBINATION AND THE FRAGILE-X | 0 | 0 |
| 710 | 8 | 33 | 710 1990 HUMAN GENETICS 85(3):267-271 LI SY; LIN JK DIFFERENTIAL BLEOMYCIN SUSCEPTIBILITY IN CULTURED LYMPHOCYTES OF FRAGILE X-PATIENTS AND NORMAL INDIVIDUALS | 3 | 5 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 711 | 9 | 21 | 711 1990 HUMAN GENETICS 85(6):590-594 YU WD; WENGER SL; STEELE MW X-CHROMOSOME IMPRINTING IN FRAGILE-X SYNDROME | 8 | 16 |
| 712 | 24 | 65 | 712 1990 HUMAN GENETICS 85(6):659-665 WOHRLE D; FRYNS JP; STEINBACH P FRAGILE-X EXPRESSION AND FRAGILE-X INACTIVATION .1. THE EXPRESSION OF THE FRAGILE SITE AT XQ27.3 IS NOT SUPPRESSED ON INACTIVE X-CHROMOSOMES SEPARATED FROM THE ACTIVE HOMOLOG | 7 | 9 |
| 713 | 18 | 36 | 713 1990 JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME 72A(6):889-896 DAVIDS JR; HAGERMAN RJ; EILERT RE ORTHOPEDIC ASPECTS OF FRAGILE-X SYNDROME | 0 | 13 |
| 714 | 0 | 1 | 714 1990 JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY AND ALLIED DISCIPLINES 31(7):1165-1166 BOLTON P THE FRAGILE X-SYNDROME - DAVIES,K | 0 | 0 |
| 715 | 0 | 0 | 715 1990 JOURNAL OF CLINICAL AND EXPERIMENTAL NEUROPSYCHOLOGY 12(1):69-69 KAUFMANN PM; LECKMAN JF; ORT SI DELAYED-RESPONSE PERFORMANCE IN MALES WITH FRAGILE-X SYNDROME | 3 | 5 |
| 716 | 0 | 0 | 716 1990 JOURNAL OF MEDICAL GENETICS 27(3):208-208 GLASS IA; WHITE EM; PIRRIT LA; BELL MV; CONNOR JM LINKAGE STUDY OF F8 IN THE FRAGILE-X SYNDROME | 0 | 0 |
| 717 | 0 | 0 | 717 1990 JOURNAL OF MEDICAL GENETICS 27(3):208-209 WEBB T PRENATAL-DIAGNOSIS OF THE FRAGILE-X SYNDROME | 0 | 0 |
| 718 | 15 | 22 | 718 1990 JOURNAL OF MENTAL DEFICIENCY RESEARCH 34:67-73 WEBB T; CRAWLEY P; BUNDEY S FOLATE TREATMENT OF A BOY WITH FRAGILE-X SYNDROME | 2 | 5 |
| 719 | 3 | 7 | 719 1990 JOURNAL OF MENTAL DEFICIENCY RESEARCH 34:81-86 COLLACOTT RA; DUCKETT DP; MATHEWS D; WARRINGTON JS; YOUNG ID DOWNS-SYNDROME AND FRAGILE-X SYNDROME IN A SINGLE PATIENT | 0 | 0 |
| 720 | 1 | 4 | 720 1990 JOURNAL OF NEUROLOGY 237(1):65-66 MUSUMECI SA; FERRI R; BERGONZI P THE SPECIFICITY OF THE CHARACTERISTIC SLEEP EEG PATTERN IN THE FRAGILE-X SYNDROME | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 721 | 6 | 24 | 721 1990 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 29(2):214-219 HODAPP RM; DYKENS EM; HAGERMAN RJ; SCHREINER R; LACHIEWICZ AM; et al. DEVELOPMENTAL IMPLICATIONS OF CHANGING TRAJECTORIES OF IQ IN MALES WITH FRAGILE-X SYNDROME | 32 | 45 |
| 722 | 11 | 26 | 722 1990 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 29(6):885-891 REISS AL; FREUND L FRAGILE X SYNDROME, DSM-III-R, AND AUTISM | 42 | 60 |
| 723 | 5 | 11 | 723 1990 JOURNAL OF THE ROYAL SOCIETY OF MEDICINE 83(1):1-2 GOODYEAR HM; SONKSON PM FRAGILE X-SYNDROME - AN IMPORTANT CAUSE OF MENTAL-RETARDATION | 0 | 0 |
| 724 | 0 | 1 | 724 1990 JOURNAL OF THE ROYAL SOCIETY OF MEDICINE 83(6):415-415 HALSTEAD S FRAGILE X-SYNDROME | 0 | 0 |
| 725 | 0 | 0 | 725 1990 JOURNAL OF THE ROYAL SOCIETY OF MEDICINE 83(6):415-415 GOODYEAR HM; SONKSON PM FRAGILE X-SYNDROME - REPLY | 0 | 0 |
| 726 | 0 | 1 | 726 1990 LANCET 336(8723):1131-1131 TEMPLE IK; BARAITSER M; PEMBREY ME; BUTLER L; JACOBS P; et al. UNUSUAL PRESENTATION OF FRAGILE-X SYNDROME | 2 | 3 |
| 727 | 3 | 10 | 727 1990 NEUROLOGY 40(2):378-380 DESAI HB; DONAT J; SHOKEIR MHK; MUNOZ DG AMYOTROPHIC LATERAL SCLEROSIS IN A PATIENT WITH FRAGILE X-SYNDROME | 5 | 7 |
| 728 | 10 | 29 | 728 1990 NEUROPSYCHOLOGIA 28(1):9-16 CROWE SF; HAY DA NEUROPSYCHOLOGICAL DIMENSIONS OF THE FRAGILE X-SYNDROME - SUPPORT FOR A NONDOMINANT HEMISPHERE DYSFUNCTION HYPOTHESIS | 38 | 54 |
| 729 | 1 | 1 | 729 1990 NUCLEIC ACIDS RESEARCH 18(3):690-690 YU S; SUTHERS GK; MULLEY JC A BCLI RFLP FOR DXS296 (VK21) NEAR THE FRAGILE-X | 2 | 6 |
| 730 | 0 | 2 | 730 1990 NUCLEIC ACIDS RESEARCH 18(3):692-692 HUPKES PE; VANBENNEKOM CA; VANOOST BA; OOSTRA BA RN1, A NEW POLYMORPHIC MARKER NEAR THE FRAGILE-X LOCUS - (HGM10 ASSIGNMENT DXS-369) | 1 | 2 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 731 | 0 | 3 | 731 1990 NUCLEIC ACIDS RESEARCH 18(20):6134-6134 WEILL D; HEYMAN T NUCLEOTIDE-SEQUENCE OF 2 PROLINE TRANSFER-RNA (AGG AND CGG) GENES FROM CHICKEN | 0 | 3 |
| 732 | 7 | 11 | 732 1990 PATHOBIOLOGY 58(4):236-240 JENKINS EC; DUNCAN CJ; SANZ MM; GENOVESE M; GU H; et al. PROGRESS TOWARD AN INTERNAL CONTROL-SYSTEM FOR FRAGILE-X INDUCTION BY 5-FLUORODEOXYURIDINE IN WHOLE-BLOOD CULTURES | 3 | 6 |
| 733 | 0 | 0 | 733 1990 PEDIATRIC RESEARCH 27(4):A12-A12 LACHIEWICZ AM; SPIRIDIGLIOZZI GA; GULLION CA; RANSFORD SK ABERRANT BEHAVIORS OF YOUNG BOYS WITH FRAGILE X-SYNDROME | 0 | 0 |
| 734 | 0 | 0 | 734 1990 PEDIATRIC RESEARCH 27(4):A136-A136 SHAPIRO LR; WILMOT PL SPONTANEOUS FRAGILE-X CHROMOSOMES IN ROUTINE AMNIOTIC-FLUID CULTURE - THE X-CHROMOSOME COMMON FRAGILE SITE [(X) (Q27.2)] MISTAKEN FOR THE FRAGILE-X CHROMOSOME [(X) (Q27.3)] | 0 | 0 |
| 735 | 0 | 0 | 735 1990 PRACTITIONER 234(1496):946-& BERNEY T FRAGILE-X SYNDROME | 0 | 0 |
| 736 | 2 | 3 | 736 1990 PRENATAL DIAGNOSIS 10(8):545-546 OOSTRA BA; SANDKUYL LA; HALLEY DJJ RISK CALCULATION OF MISSED PRENATAL-DIAGNOSIS OF FRAGILE-X SYNDROME | 1 | 1 |
| 737 | 0 | 0 | 737 1990 PRENATAL DIAGNOSIS 10(8):546-546 WEBB TP RISK CALCULATION OF MISSED PRENATAL-DIAGNOSIS OF FRAGILE-X SYNDROME - REPLY | 0 | 0 |
| 738 | 3 | 18 | 738 1990 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 87(10):3856-3860 WARREN ST; KNIGHT SJL; PETERS JF; STAYTON CL; CONSALEZ GG; et al. ISOLATION OF THE HUMAN CHROMOSOMAL BAND XQ28 WITHIN SOMATIC-CELL HYBRIDS BY FRAGILE X-SITE BREAKAGE | 24 | 69 |
| 739 | 7 | 34 | 739 1990 YALE JOURNAL OF BIOLOGY AND MEDICINE 63(4):293-299 BREGMAN JD; LECKMAN JF; ORT SI THYROID-FUNCTION IN FRAGILE-X SYNDROME MALES | 6 | 8 |
| 740 | 7 | 17 | 740 1991 AMERICAN JOURNAL OF HUMAN GENETICS 48(1):108-116 ROUSSEAU F; VINCENT A; RIVELLA S; HEITZ D; TRIBOLI C; et al. 4 CHROMOSOMAL BREAKPOINTS AND 4 NEW PROBES MARK OUT A 10-CM REGION ENCOMPASSING THE FRAGILE-X LOCUS (FRAXA) | 25 | 48 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 741 | 22 | 49 | 741 1991 AMERICAN JOURNAL OF HUMAN GENETICS 48(2):195-202 COHEN IL; SUDHALTER V; PFADT A; JENKINS EC; BROWN WT; et al. WHY ARE AUTISM AND THE FRAGILE-X SYNDROME ASSOCIATED - CONCEPTUAL AND METHODOLOGICAL ISSUES | 34 | 65 |
| 742 | 16 | 33 | 742 1991 AMERICAN JOURNAL OF HUMAN GENETICS 48(3):460-467 SUTHERS GK; MULLEY JC; VOELCKEL MA; DAHL N; VAISANEN ML; et al. GENETIC-MAPPING OF NEW DNA PROBES AT XQ27 DEFINES A STRATEGY FOR DNA STUDIES IN THE FRAGILE-X SYNDROME | 30 | 47 |
| 743 | 0 | 1 | 743 1991 AMERICAN JOURNAL OF HUMAN GENETICS 48(4):815-815 FINUCANE B; SCOTT CI; KURTZ MB CONCURRENCE OF DOMINANT PIEBALD TRAIT AND FRAGILE X-SYNDROME | 0 | 2 |
| 744 | 6 | 17 | 744 1991 AMERICAN JOURNAL OF HUMAN GENETICS 48(6):1051-1057 RICHARDS RI; SHEN Y; HOLMAN K; KOZMAN H; HYLAND VJ; et al. FRAGILE-X SYNDROME - DIAGNOSIS USING HIGHLY POLYMORPHIC MICROSATELLITE MARKERS | 15 | 40 |
| 745 | 17 | 34 | 745 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(2):279-288 REISS AL; FREUND L; TSENG JE; JOSHI PK NEUROANATOMY IN FRAGILE-X FEMALES - THE POSTERIOR-FOSSA | 44 | 64 |
| 746 | 10 | 22 | 746 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(3):656-661 KREMER EJ; YU S; PRITCHARD M; NAGARAJA R; HEITZ D; et al. ISOLATION OF A HUMAN DNA-SEQUENCE WHICH SPANS THE FRAGILE-X | 21 | 32 |
| 747 | 0 | 0 | 747 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):35-35 TURNER G FRAGILE X-SYNDROME | 0 | 0 |
| 748 | 0 | 1 | 748 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):75-75 SCHLESSINGER D; ZUCCHI I; NAGARAJA R; LITTLE RD; ABIDI F; et al. CLONING OF THE FRAGILE-X LOCUS IN THE CONTEXT OF YEAST ARTIFICIAL CHROMOSOME-BASED MAPPING OF XQ24-28 | 0 | 0 |
| 749 | 0 | 0 | 749 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):75-75 POUSTKA A; DIETRICH A; KORN B; GROSS B; MONACO A; et al. MOLECULAR CHARACTERIZATION OF THE FRAGILE-X REGION | 0 | 0 |
| 750 | 0 | 0 | 750 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):75-75 KUHL D; PIERETTI M; REINER O; NELSON D FRAGILE-X SITE - MOLECULAR AND GENETIC-CHARACTERIZATION | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 751 | 0 | 0 | 751 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):76-76 OBERLE I; ROUSSEAU F; HEITZ D; DEVYS D; ZENGERLING S; et al. MOLECULAR-BASIS OF THE FRAGILE-X SYNDROME AND DIAGNOSTIC APPLICATIONS | 0 | 0 |
| 752 | 0 | 0 | 752 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):76-76 YU S; KREMER E; PRITCHARD M; LYNCH M; NANCARROW J; et al. THE FRAGILE-X GENOTYPE IS CHARACTERIZED BY AN UNSTABLE REGION OF DNA | 0 | 0 |
| 753 | 0 | 0 | 753 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):103-103 ROCCHI M; MORABITO E; DINATALE P IDURONATE SULFATASE ACTIVITY ON LYMPHOBLASTOID CELL-LINES FROM SUBJECTS AFFECTED BY FRAGILE-X SYNDROME | 0 | 0 |
| 754 | 0 | 0 | 754 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):139-139 HAGERMAN RJ; BRUNSCHWIG A; MILLER L; BUTLER MG SELECTED STANDARDS FOR ANTHROPOMETRIC MEASUREMENTS IN FRAGILE X-SYNDROME | 0 | 0 |
| 755 | 0 | 0 | 755 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):158-158 RAMZY MI; SALINAS CF ORODENTAL FINDINGS IN AN EGYPTIAN SAMPLE OF FRAGILE-X CASES | 0 | 0 |
| 756 | 0 | 0 | 756 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):159-159 REISS A; FREUND L; AYLWARD E NEUROANATOMY OF THE FRAGILE X SYNDROME | 0 | 0 |
| 757 | 0 | 0 | 757 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):163-163 SEEMANOVA E; GOETZ P; SVOBODOVA M; LESNY I INCESTUOUS MATINGS IN FAMILIES WITH FRAGILE (X) SYNDROME | 0 | 0 |
| 758 | 0 | 0 | 758 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):194-194 KUHL DPA; WARREN ST; RIGGINS GJ; NELSON DL; CASKEY CT USE OF CA REPEAT MARKER DXS548 FOR PRENATAL-DIAGNOSIS OF FRAGILE-X SYNDROME AND THE IDENTIFICATION OF NEW POSSIBLY POLYMORPHIC SITES IN THE FRAGILE-X REGION | 0 | 0 |
| 759 | 0 | 0 | 759 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):211-211 BROWN WT; GOONEWARDENA P; RAY J; MIEZEJESKI C; KRAWCZUN M; et al. PRENATALLY DETECTED FRAGILE X FEMALES - COUNSELING ISSUES AND LONG-TERM FOLLOW-UPS | 0 | 0 |
| 760 | 0 | 0 | 760 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):221-221 KAHKONEN M; VAISANEN ML; WINGVIST R; LEISTI J PRENATAL-DIAGNOSIS OF FRAGILE X SYNDROME | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 761 | 0 | 0 | 761 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):231-231 SHAPIRO LR; WILMOT PL PRENATAL CYTOGENETIC DIAGNOSIS OF THE FRAGILE X-SYNDROME - DETERMINATION OF ACCURACY | 1 | 1 |
| 762 | 0 | 0 | 762 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):235-235 LI Q; XU DD; ZHOU LY FRAGILE X-FREQUENCY IN MENTALLY-RETARDED CHILDREN AND IN FETAL BLOOD BY CORDOCENTESIS | 0 | 0 |
| 763 | 0 | 0 | 763 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):257-257 JACKSONCOOK J; PISERCHIO C; VIRGINIA J MOSAIC XY/XYY AND FRAGILE-X IN A 4-YEAR-OLD MALE BODURTHA | 0 | 0 |
| 764 | 0 | 0 | 764 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):267-267 KARIMINEJAD MH; RAHIMI M; SHIRNESHAN K; VAEZI SA; KARIMINEJAD R FRAGILE-X (BELL,MARTIN) SYNDROME IN AN IRANIAN FAMILY WITH 8 AFFECTED MEMBERS | 0 | 0 |
| 765 | 0 | 0 | 765 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):269-269 LOZZIO CB; MATTESON K; CACHEIRO NL CARRIER DETECTION OF FRAGILE-X USING TRIMETHOPRIM AND DNA LINKAGE ANALYSES | 0 | 0 |
| 766 | 0 | 0 | 766 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):269-269 PAJARES IL; DELICADO A; DETORRES ML; MARTIN VL; CASTROVIEJO IP; et al. FRAGILE-X SYNDROME WITH EXTRAMICROCHROMOSOME | 0 | 0 |
| 767 | 0 | 1 | 767 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):270-270 MURTHY SK; KAR B FRAGILE-X SYNDROME IN MENTALLY-RETARDED POPULATION OF WESTERN INDIA | 0 | 0 |
| 768 | 0 | 0 | 768 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):273-273 RISCILE GR FRAGILE-X PATIENTS WITH ATYPICAL PHENOTYPES | 0 | 0 |
| 769 | 0 | 0 | 769 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):280-280 ZASLAV AL; BROWN WT THE SIGNIFICANCE OF LOW-LEVEL FRAGILE X EXPRESSION | 0 | 0 |
| 770 | 0 | 0 | 770 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):287-287 RAFI SK; SURANA RB; ANDERSON LH; CHRISTOPHER KL; WILSON B; et al. HYPEROXIA ENHANCES THE INDUCTION OF FRAGILE-X SITE OF THE FRAGILE-X SYNDROME | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 771 | 0 | 0 | 771 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):289-289 BUCKLEY D; JALAL S; DEWALD G FRAGILE-X STUDIES - WHAT IS PRACTICAL | 0 | 0 |
| 772 | 0 | 0 | 772 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):290-290 JENKINS E; GENOVESE M; DUNCAN C; GU H; SCHWARTZRICHSTEIN C; et al. COMMON FRAGILE SITE FRA(X)(Q27.2), PRESENT IN ONLY 1 OF 685 CASES SCREENED FOR THE FRAGILE-X SYNDROME | 0 | 0 |
| 773 | 0 | 0 | 773 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):290-290 HOWARDPEEBLES PN FRAGILE-X TESTING OF FAMILY MEMBERS IN THE CLINICAL CYTOGENETICS LABORATORY - PERIMETERS AND PITFALLS | 0 | 0 |
| 774 | 0 | 0 | 774 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):291-291 LOGHINGROSSO NS; LAUANDOS JE; ALI VRA; GRACA CHN; SCHMIDT BJ SEARCHING FOR FRAGILE-X IN AN INSTITUTION FOR MENTALLY-HANDICAPPED IN BRAZIL | 0 | 0 |
| 775 | 0 | 0 | 775 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):292-292 SHAPIRO LR; PETRELLA R; EALLONARDO SJ; WILMOT PL RELIABILITY OF OTHER FOLATE SENSITIVE FRAGILE SITE EXPRESSION AS AN INDICATION OF SUCCESSFUL INDUCTION OF THE FRAGILE-X CHROMOSOME | 0 | 0 |
| 776 | 0 | 0 | 776 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):293-293 TENGSTROM C; AUTIO S CHROMOSOMAL-ABERRATIONS IN 542 MENTALLY-RETARDED PATIENTS EXAMINED BY HIGH-RESOLUTION BANDING INCLUDING FRAGILE X-SCREENING | 0 | 0 |
| 777 | 0 | 0 | 777 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):303-303 MCCOMBS J; ROUSE B; LOCKHART L; HOWARDPEEBLES P PRENATAL IDENTIFICATION OF FRAGILE-X AND A MARKER CHROMOSOME | 0 | 0 |
| 778 | 0 | 0 | 778 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):331-331 TURNER G; ROBINSON H; LAING S; SHERMAN S SCREENING FOR THE FRAGILE X-SYNDROME - IMPACT OF GENETIC-COUNSELING ON REPRODUCTIVE CHOICES OF WOMEN AT RISK FOR HAVING AN AFFECTED CHILD | 0 | 0 |
| 779 | 0 | 0 | 779 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):338-338 GLASS IA; DELMASTRO RG; LANYON WG; RAEBURN JA; KILPATRICK MW; et al. IDENTIFICATION OF DIAGNOSTIC DNA MARKERS FOR THE FRAGILE-X SYNDROME | 0 | 0 |
| 780 | 0 | 0 | 780 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):341-341 GOONEWARDENA P; GLICKSMAN A; BROWN WT LINKAGE ANALYSIS OF PROXIMAL DNA MARKERS RN1 AND VK23 USED IN THE DIAGNOSIS OF FRAGILE-X SYNDROME | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 781 | 0 | 0 | 781 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):353-353 NORDSTROM AM; VONKOSKULL H LINKAGE TO DXS52 IN A FRAGILE-X NEGATIVE FAMILY | 0 | 0 |
| 782 | 0 | 0 | 782 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):357-357 RIGGINS GJ; SHERMAN SL; OOSTRA BA; FEITELL D; SUTCLIFFE JS; et al. A FREQUENT DINUCLEOTIDE POLYMORPHISM OF THE FRAGILE-X BREAKPOINT CLUSTER REGION IS TIGHTLY LINKED TO THE FRAGILE-X SYNDROME LOCUS | 0 | 0 |
| 783 | 0 | 0 | 783 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):383-383 LEE JT; MURGIA A; WARREN S; NELSON D; NUSSBAUM R CONSTRUCTION OF A 600-KB YAC CONTIG PROXIMAL TO THE FRAGILE X-SITE | 0 | 0 |
| 784 | 0 | 0 | 784 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):417-417 REINER O; VERKERK AJMH; PIERETTI M; PIZZUTI A; BLONDE L; et al. CHARACTERIZATION OF EXPRESSED SEQUENCES AT THE FRAGILE-X LOCUS | 0 | 0 |
| 785 | 0 | 0 | 785 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):469-469 FISCH GS; SHAPIRO LR; SIMENSEN R; SCHWARTZ CE; FRYNS JP; et al. DIFFERENCES IN DECLINE IN IQ AMONG FRAGILE-X MALES - EVIDENCE FOR GENETIC-HETEROGENEITY | 0 | 0 |
| 786 | 0 | 0 | 786 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):474-474 LOESCH DZ; HUGGINS R ESTIMATION OF THE EFFECTS OF FRAGILE-X ON DISTRIBUTIONS OF PHYSICAL AND INTELLECTUAL MEASURES USING A MAXIMUM-LIKELIHOOD SCORING TECHNIQUE | 0 | 0 |
| 787 | 12 | 39 | 787 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):158-172 BROWN WT; JENKINS E; NERI G; LUBS H; SHAPIRO LR; et al. 4TH INTERNATIONAL WORKSHOP ON THE FRAGILE-X AND X-LINKED MENTAL-RETARDATION | 1 | 7 |
| 788 | 0 | 0 | 788 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 |
| 789 | 12 | 19 | 789 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):251-255 NOLIN SL; SNIDER DA; JENKINS EC; BROWN WT; KRAWCZUN M; et al. FRAGILE-X SCREENING-PROGRAM IN NEW-YORK-STATE | 18 | 24 |
| 790 | 1 | 1 | 790 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 791 | 7 | 32 | 791 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):260-268 BUTLER MG; ALLEN GA; HAYNES JL; SINGH DN; WATSON MS; et al. ANTHROPOMETRIC COMPARISON OF MENTALLY-RETARDED MALES WITH AND WITHOUT THE FRAGILE-X SYNDROME | 16 | 22 |
| 792 | 11 | 14 | 792 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):269-274 CRONISTER A; SCHREINER R; WITTENBERGER M; AMIRI K; HARRIS K; et al. HETEROZYGOUS FRAGILE-X FEMALE - HISTORICAL, PHYSICAL, COGNITIVE, AND CYTOGENETIC FEATURES | 39 | 57 |
| 793 | 12 | 21 | 793 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):283-287 HAGERMAN RJ; AMIRI K; CRONISTER A FRAGILE-X CHECKLIST | 47 | 64 |
| 794 | 1 | 8 | 794 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):288-289 ZHAO Y; SHEN Y; LIU Y; ZHANG JC; YE LZ; et al. FRAGILE-X SYNDROME (MARTIN-BELL SYNDROME) IN CHINA | 1 | 1 |
| 795 | 12 | 23 | 795 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):292-297 BROWN WT; GROSS A; GOONEWARDENA P; FERRANDO C; DOBKIN C; et al. DETECTION OF FRAGILE-X NON-PENETRANT MALES BY DNA MARKER ANALYSIS | 4 | 4 |
| 796 | 16 | 47 | 796 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):298-304 GLASS IA; PIRRIT LA; WHITE EM; BELL MV; DAVIES KE; et al. LINKAGE ANALYSIS IN THE FRAGILE-X SYNDROME USING MULTIPLE DISTAL XQ POLYMORPHIC DNA MARKERS | 2 | 2 |
| 797 | 2 | 9 | 797 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 |
| 798 | 7 | 20 | 798 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 |
| 799 | 9 | 14 | 799 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):319-321 DAHL N; MALMGREN H; PETTERSSON U; HOLMGREN G; SEEMANOVA E; et al. CARRIER DETECTION OF THE FRAGILE-X SYNDROME USING FLANKING LOCI DXS98, DXS105, AND DXS304 | 0 | 0 |
| 800 | 14 | 31 | 800 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):322-327 GOONEWARDENA P; BROWN WT; GROSS AC; FERRANDO C; DOBKIN C; et al. LINKAGE ANALYSIS OF THE FRAGILE-X SYNDROME USING A NEW DNA MARKER U6.2 DEFINING LOCUS DXS304 | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 801 | 6 | 18 | 801 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):328-331 VANOOST BA; SMITS A; DREESEN JCFM; SMEETS D; PERDON L; et al. MULTIPOINT LINKAGE ANALYSIS OF DXS369 AND DXS304 IN FRAGILE-X FAMILIES | 4 | 7 |
| 802 | 3 | 20 | 802 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):343-346 BROWN WT; GROSS AC; GOONEWARDENA P; FERRANDO C; DOBKIN C; et al. LINKAGE IN FRAGILE-X FAMILIES OF 3 DISTAL FLANKING MARKERS - ST14, DX13, AND F8 | 1 | 2 |
| 803 | 4 | 4 | 803 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):347-348 ROMANO V; MASCALI G; CHIAVETTA V; RAGUSA RM; BARLETTA C; et al. RFLP ANALYSIS IN 5 SICILIAN FAMILIES WITH THE FRAGILE-X SYNDROME | 0 | 0 |
| 804 | 16 | 20 | 804 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 |
| 805 | 7 | 11 | 805 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 |
| 806 | 12 | 18 | 806 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 |
| 807 | 13 | 23 | 807 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):370-373 BROOKS SS; COHEN I; FERRANDO C; JENKINS EC; BROWN WT; et al. CYTOGENETICALLY NEGATIVE, LINKAGE POSITIVE FRAGILE-X SYNDROME | 0 | 1 |
| 808 | 13 | 25 | 808 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):374-377 VOELCKEL MA; PELLISSIER MC; PIQUET C; NGUYEN C; BOCCACCIO I; et al. FRAGILE-X SYNDROME IN AN EXTENDED FAMILY WITH SPECIAL REFERENCE TO AN AFFECTED MALE WITH KLINEFELTER SYNDROME | 2 | 2 |
| 809 | 1 | 5 | 809 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 |
| 810 | 4 | 15 | 810 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):380-383 PERGOLIZZI R; BROWN WT; GOONEWARDENA P; BHAN R; DOBKIN C; et al. MOLECULAR CHARACTERIZATION OF A DNA PROBE, U6.2, LOCATED CLOSE TO THE FRAGILE-X LOCUS | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 811 | 11 | 25 | 811 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 |
| 812 | 4 | 7 | 812 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 |
| 813 | 4 | 23 | 813 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):400-403 JACKY PB; AHUJA YR; ANYANEYEBOA K; BREG WR; CARPENTER NJ; et al. GUIDELINES FOR THE PREPARATION AND ANALYSIS OF THE FRAGILE-X CHROMOSOME IN LYMPHOCYTES | 31 | 44 |
| 814 | 7 | 16 | 814 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 |
| 815 | 0 | 4 | 815 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 |
| 816 | 1 | 7 | 816 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 |
| 817 | 4 | 16 | 817 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 |
| 818 | 12 | 22 | 818 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 | 4 | 5 |
| 819 | 6 | 20 | 819 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):429-433 KIMCHISARFATY C; GOITEIN R; KEREM B; WERNER M; MEIDAN B; et al. ENDOREDUPLICATION AND POLYPLOIDY IN FRAGILE-X CELLS INDUCED BY METHOTREXATE AND FLUORODEOXYURIDINE - IMPLICATIONS FOR DIAGNOSIS | 1 | 3 |
| 820 | 10 | 28 | 820 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 821 | 2 | 4 | 821 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):445-446 HOWARDPEEBLES PN FRAGILE-X EXPRESSION - USE OF A DOUBLE INDUCTION SYSTEM | 2 | 4 |
| 822 | 4 | 11 | 822 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 |
| 823 | 2 | 33 | 823 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):456-463 KRAWCZUN MS; JENKINS EC; DUNCAN CJ; STARKHOUCK SL; KUNAPORN S; et al. DISTRIBUTION OF AUTOSOMAL FRAGILE SITES IN SPECIMENS CULTURED FOR PRENATAL FRAGILE-X DIAGNOSIS | 1 | 1 |
| 824 | 1 | 8 | 824 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):464-466 JENKINS EC; BROOKS SE; STARKHOUCK SL; DUNCAN CJ; BROOKS SLS; et al. SV40-TRANSFORMED FRAGILE(X) AMNIOCYTES | 1 | 1 |
| 825 | 9 | 34 | 825 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):481-487 FISCH GS; ARINAMI T; FROSTERISKENIUS U; FRYNS JP; CURFS LM; et al. RELATIONSHIP BETWEEN AGE AND IQ AMONG FRAGILE-X MALES - A MULTICENTER STUDY | 13 | 14 |
| 826 | 6 | 20 | 826 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 | 7 | 9 |
| 827 | 3 | 21 | 827 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 | 23 | 31 |
| 828 | 3 | 19 | 828 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 |
| 829 | 7 | 15 | 829 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 |
| 830 | 7 | 12 | 830 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 | 21 | 25 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 831 | 3 | 9 | 831 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):509-509 HECHT F SEIZURE DISORDERS IN THE FRAGILE-X CHROMOSOME SYNDROME | 3 | 7 |
| 832 | 3 | 10 | 832 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):511-513 MUSUMECI SA; FERRI R; ELIA M; COLOGNOLA RM; BERGONZI P; et al. EPILEPSY AND FRAGILE-X SYNDROME - A FOLLOW-UP-STUDY | 21 | 36 |
| 833 | 5 | 15 | 833 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 |
| 834 | 14 | 31 | 834 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 40(2):234-243 CIANCHETTI C; SANNIOFANCELLO G; FRATTA AL; MANCONI F; ORANO A; et al. NEUROPSYCHOLOGICAL, PSYCHIATRIC, AND PHYSICAL MANIFESTATIONS IN 149 MEMBERS FROM 18 FRAGILE-X FAMILIES | 16 | 19 |
| 835 | 2 | 4 | 835 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 |
| 836 | 2 | 5 | 836 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 |
| 837 | 2 | 12 | 837 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 |
| 838 | 10 | 39 | 838 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 | 92 | 134 |
| 839 | 1 | 15 | 839 1991 ANNALES DE GENETIQUE 34(2):111-114 BARLETTA C; RAGUSA RM; GAROFALO G; SCILLATO F; RUGGERI M SEGREGATION ANALYSIS OF AUTOSOMAL FRAGILE SITES IN 3 FAMILIES WITH THE FRAGILE X-CHROMOSOME | 0 | 5 |
| 840 | 4 | 31 | 840 1991 ANNALS OF NEUROLOGY 29(1):26-32 REISS AL; AYLWARD E; FREUND LS; JOSHI PK; BRYAN RN NEUROANATOMY OF FRAGILE-X-SYNDROME - THE POSTERIOR-FOSSA | 60 | 114 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 841 | 0 | 0 | 841 1991 ANNALS OF NEUROLOGY 30(3):450-450 BERRYKRAVIS E; HODGES C DEMONSTRATION OF ABNORMAL CYCLIC ADENOSINE-MONOPHOSPHATE PRODUCTION IN MULTIPLE TISSUES FROM INDIVIDUALS WITH FRAGILE X-SYNDROME | 0 | 0 |
| 842 | 16 | 38 | 842 1991 BIOESSAYS 13(5):243-251 JORDAN BR FRAGILE X-LINKED MENTAL-RETARDATION AND THE DIFFICULTIES OF REVERSE GENETICS | 1 | 1 |
| 843 | 5 | 13 | 843 1991 BIOLOGICAL PSYCHIATRY 29(3):298-299 MENDLEWICZ J; HIRSCH D BIPOLAR MANIC-DEPRESSIVE ILLNESS AND THE FRAGILE-X SYNDROME | 0 | 1 |
| 844 | 1 | 2 | 844 1991 BRITISH MEDICAL JOURNAL 302(6789):1359-1359 CHARATAN F GENE FOR FRAGILE-X SYNDROME DISCOVERED | 0 | 0 |
| 845 | 9 | 34 | 845 1991 CELL 64(4):861-866 BELL MV; HIRST MC; NAKAHORI Y; MACKINNON RN; ROCHE A; et al. PHYSICAL MAPPING ACROSS THE FRAGILE-X - HYPERMETHYLATION AND CLINICAL EXPRESSION OF THE FRAGILE-X SYNDROME | 127 | 224 |
| 846 | 11 | 40 | 846 1991 CELL 65(5):905-914 VERKERK AJMH; PIERETTI M; SUTCLIFFE JS; FU YH; KUHL DPA; et al. IDENTIFICATION OF A GENE (FMR-1) CONTAINING A CGG REPEAT COINCIDENT WITH A BREAKPOINT CLUSTER REGION EXHIBITING LENGTH VARIATION IN FRAGILE-X SYNDROME | 576 | 1282 |
| 847 | 10 | 15 | 847 1991 CELL 66(4):817-822 PIERETTI M; ZHANG FP; FU YH; WARREN ST; OOSTRA BA; et al. ABSENCE OF EXPRESSION OF THE FMR-1 GENE IN FRAGILE-X SYNDROME | 333 | 598 |
| 848 | 12 | 23 | 848 1991 CELL 67(6):1047-1058 FU YH; KUHL DPA; PIZZUTI A; PIERETTI M; SUTCLIFFE JS; et al. VARIATION OF THE CGG REPEAT AT THE FRAGILE-X SITE RESULTS IN GENETIC INSTABILITY - RESOLUTION OF THE SHERMAN PARADOX | 432 | 957 |
| 849 | 5 | 10 | 849 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 |
| 850 | 4 | 13 | 850 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 851 | 0 | 0 | 851 1991 CLINICAL RESEARCH 39(1):A1-A1 GOLDSON E; HAGERMAN RJ TEMPERAMENT AND THE FRAGILE-X SYNDROME | 2 | 2 |
| 852 | 0 | 0 | 852 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 |
| 853 | 9 | 28 | 853 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 |
| 854 | 0 | 2 | 854 1991 CYTOGENETICS AND CELL GENETICS 56(3-4):221-221 HOWARDPEEBLES PN FRAGILE X SCREENING VS FAMILY STUDIES (ESPECIALLY IN FEMALES) - LABORATORY PROCEDURES GUIDELINES | 0 | 0 |
| 855 | 0 | 0 | 855 1991 CYTOGENETICS AND CELL GENETICS 56(3-4):221-221 SHAPIRO LR; EALLONARDO SJ; WILMOT PL INTERNAL CONTROL FOR SUCCESSFUL INDUCTION OF THE FRAGILE X-CHROMOSOME - OTHER FOLATE SENSITIVE FRAGILE SITE EXPRESSION ELIMINATED | 1 | 1 |
| 856 | 2 | 9 | 856 1991 CYTOGENETICS AND CELL GENETICS 58(3-4):2054-2055 BOUVET A; BASRUR PK A MARKER FRAGILE X-CHROMOSOME ASSOCIATED WITH BALDY CALF SYNDROME | 1 | 1 |
| 857 | 0 | 0 | 857 1991 CYTOGENETICS AND CELL GENETICS 58(3-4):2062-2062 DJABALI M; NGUYEN C; BIUNNO I; IKEDA JE; OOSTRA BA; et al. LASER MICRODISSECTION OF THE FRAGILE-X REGION ALLOWS ISOLATION OF COSMID CLONES CONTAINING CONSERVED SEQUENCES | 0 | 0 |
| 858 | 0 | 2 | 858 1991 CYTOGENETICS AND CELL GENETICS 58(3-4):2062-2062 DIETRICH A; LANGENSTEIN G; TONIOLO D; WARREN ST; LEHRACH H; et al. A PHYSICAL MAP OF THE HUMAN XQ27-QTER - LOCALIZING THE REGION OF THE FRAGILE-X MUTATION | 0 | 0 |
| 859 | 2 | 5 | 859 1991 CYTOGENETICS AND CELL GENETICS 58(3-4):2065-2065 GRAHAM CA; GRIER DG; CLARKSON M; STEWART FJ; NEVIN NC LINKAGE ANALYSIS IN FRAGILE-X SYNDROME | 0 | 0 |
| 860 | 2 | 5 | 860 1991 CYTOGENETICS AND CELL GENETICS 58(3-4):2067-2067 HIRST M; NAKAHORI Y; KNIGHT S; ROCHE A; RAUT C; et al. A YAC CONTIG ACROSS THE FRAGILE-X REGION DERIVED FROM CHROMOSOME MICRODISSECTION MARKERS | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 861 | 0 | 0 | 861 1991 CYTOGENETICS AND CELL GENETICS 58(3-4):2076-2076 LYNCH M; KREMER EJ; PRITCHARD MA; YU S; BAKER E; et al. THE FRAGILE-X GENOTYPE IS CHARACTERIZED BY AN UNSTABLE REGION OF DNA | 0 | 0 |
| 862 | 0 | 4 | 862 1991 CYTOGENETICS AND CELL GENETICS 58(3-4):2082-2082 POUSTKA A; DIETRICH A; KIOSCHIS P; KORN B; GROSS B; et al. MOLECULAR CHARACTERIZATION OF THE FRAGILE-X REGION | 0 | 0 |
| 863 | 1 | 3 | 863 1991 CYTOGENETICS AND CELL GENETICS 58(3-4):2085-2085 RIGGINS GJ; SHERMAN SL; OOSTRA BA; FEITELL D; SUTCLIFFE JS; et al. A HIGHLY POLYMORPHIC DINUCLEOTIDE REPEAT, DXS 548, IS TIGHTLY LINKED TO THE FRAGILE-X SITE | 1 | 2 |
| 864 | 12 | 47 | 864 1991 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 33(9):776-788 FERRIER LJ; BASHIR AS; MERYASH DL; JOHNSTON J; WOLFF P CONVERSATIONAL SKILLS OF INDIVIDUALS WITH FRAGILE-X SYNDROME - A COMPARISON WITH AUTISM AND DOWN-SYNDROME | 21 | 25 |
| 865 | 18 | 35 | 865 1991 GENOMICS 10(3):576-582 SUTHERS GK; MULLEY JC; VOELCKEL MA; DAHL N; VAISANEN ML; et al. LINKAGE HOMOGENEITY NEAR THE FRAGILE-X LOCUS IN NORMAL AND FRAGILE-X FAMILIES | 9 | 13 |
| 866 | 9 | 23 | 866 1991 GENOMICS 10(4):1053-1060 DJABALI M; NGUYEN C; BIUNNO I; OOSTRA BA; MATTEI MG; et al. LASER MICRODISSECTION OF THE FRAGILE X REGION - IDENTIFICATION OF COSMID CLONES AND OF CONSERVED SEQUENCES IN THIS REGION | 1 | 25 |
| 867 | 2 | 8 | 867 1991 HUMAN GENETICS 87(1):95-96 KAHKONEN M; HAATAJA R; LEISTI J URIDINE ENHANCES EXPRESSION OF THE FRAGILE-X CHROMOSOME IN HUMAN-LYMPHOCYTES | 2 | 2 |
| 868 | 7 | 16 | 868 1991 HUMAN GENETICS 87(3):369-372 HULSEBOS TJM; OOSTRA BA; BROERSEN S; SMITS A; VANOOST BA; et al. NEW DISTAL MARKER CLOSELY LINKED TO THE FRAGILE-X LOCUS | 4 | 13 |
| 869 | 9 | 24 | 869 1991 HUMAN GENETICS 87(4):421-424 WOHRLE D; STEINBACH P FRAGILE-X EXPRESSION AND X-INACTIVATION .2. THE FRAGILE SITE AT XQ27.3 HAS A BASIC FUNCTION IN THE PATHOGENESIS OF FRAGILE X-LINKED MENTAL-RETARDATION | 6 | 8 |
| 870 | 5 | 10 | 870 1991 HUMAN GENETICS 87(4):503-505 STEEN AM; MARCUS S; SAHLEN S; NIELSEN KB; LAMBERT B THE FRAGILE-X MUTATION DOES NOT HAVE ANY MAJOR EFFECT ON THE EXPRESSION OF THE HYPOXANTHINE PHOSPHORIBOSYLTRANSFERASE (HPRT) LOCUS IN HUMAN FIBROBLASTS | 0 | 2 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 871 | 9 | 23 | 871 1991 JOURNAL OF ABNORMAL CHILD PSYCHOLOGY 19(3):253-262 EINFELD S; HALL W; LEVY F HYPERACTIVITY AND THE FRAGILE X SYNDROME | 12 | 13 |
| 872 | 6 | 28 | 872 1991 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 21(4):503-516 HODAPP RM; DYKENS EM; ORT SI; ZELINSKY DG; LECKMAN JF CHANGING PATTERNS OF INTELLECTUAL STRENGTHS AND WEAKNESSES IN MALES WITH FRAGILE-X SYNDROME | 5 | 16 |
| 873 | 4 | 15 | 873 1991 JOURNAL OF CLINICAL PSYCHOPHARMACOLOGY 11(6):398-399 COHEN IL; TSIOURIS JA; PFADT A EFFECTS OF LONG-ACTING PROPRANOLOL ON AGONISTIC AND STEREOTYPED BEHAVIORS IN A MAN WITH PERVASIVE DEVELOPMENTAL DISORDER AND FRAGILE-X SYNDROME - A DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY | 2 | 5 |
| 874 | 4 | 4 | 874 1991 JOURNAL OF MEDICAL GENETICS 28(5):358-358 WEBB T; BUNDEY S PREVALENCE OF FRAGILE X-SYNDROME | 6 | 8 |
| 875 | 0 | 0 | 875 1991 JOURNAL OF MEDICAL GENETICS 28(12):809-810 JACOBS PA THE FRAGILE-X SYNDROME | 6 | 10 |
| 876 | 6 | 9 | 876 1991 JOURNAL OF MEDICAL GENETICS 28(12):811-813 CONNOR JM CLONING OF THE GENE FOR THE FRAGILE-X SYNDROME - IMPLICATIONS FOR THE CLINICAL GENETICIST | 1 | 1 |
| 877 | 6 | 6 | 877 1991 JOURNAL OF MEDICAL GENETICS 28(12):814-817 WEBB T MOLECULAR-GENETICS OF FRAGILE-X - A CYTOGENETICS VIEWPOINT - REPORT OF THE 5TH INTERNATIONAL-SYMPOSIUM ON X-LINKED MENTAL-RETARDATION, STRASBOURG, FRANCE, 12 TO 16 AUGUST 1991 | 3 | 7 |
| 878 | 5 | 10 | 878 1991 JOURNAL OF MEDICAL GENETICS 28(12):818-823 RICHARDS RI; HOLMAN K; KOZMAN H; KREMER E; LYNCH M; et al. FRAGILE-X SYNDROME - GENETIC LOCALIZATION BY LINKAGE MAPPING OF 2 MICROSATELLITE REPEATS FRAXAC1 AND FRAXAC2 WHICH IMMEDIATELY FLANK THE FRAGILE SITE | 63 | 102 |
| 879 | 11 | 17 | 879 1991 JOURNAL OF MEDICAL GENETICS 28(12):824-829 HIRST MC; NAKAHORI Y; KNIGHT SJL; SCHWARTZ C; THIBODEAU SN; et al. GENOTYPE PREDICTION IN THE FRAGILE-X SYNDROME | 27 | 36 |
| 880 | 11 | 20 | 880 1991 JOURNAL OF MEDICAL GENETICS 28(12):830-836 ROUSSEAU F; HEITZ D; OBERLE I; MANDEL JL SELECTION IN BLOOD-CELLS FROM FEMALE CARRIERS OF THE FRAGILE-X SYNDROME - INVERSE CORRELATION BETWEEN AGE AND PROPORTION OF ACTIVE X-CHROMOSOMES CARRYING THE FULL MUTATION | 64 | 86 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 881 | 1 | 6 | 881 1991 JOURNAL OF MEDICAL GENETICS 28(12):837-839 GRIFFITHS MJ; STRACHAN MC A SINGLE LYMPHOCYTE CULTURE FOR FRAGILE-X INDUCTION AND PROMETAPHASE CHROMOSOME ANALYSIS | 0 | 1 |
| 882 | 2 | 8 | 882 1991 JOURNAL OF REPRODUCTION AND FERTILITY 91(1):203-206 TEWARI R; RAO SRV REPLICATION STATUS OF THE FRAGILE X-CHROMOSOME AND ITS IMPLICATIONS FOR REPRODUCTIVE-PERFORMANCE IN THE INDIAN MOLE RAT (NESOKIA-INDICA) | 0 | 0 |
| 883 | 24 | 53 | 883 1991 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 30(5):825-830 PIVEN J; GAYLE J; LANDA R; WZOREK M; FOLSTEIN S THE PREVALENCE OF FRAGILE-X IN A SAMPLE OF AUTISTIC INDIVIDUALS DIAGNOSED USING A STANDARDIZED INTERVIEW | 7 | 26 |
| 884 | 9 | 18 | 884 1991 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 30(5):831-834 HILTON DK; MARTIN CA; HEFFRON WM; HALL BD; JOHNSON GL IMIPRAMINE TREATMENT OF ADHD IN A FRAGILE-X CHILD | 5 | 10 |
| 885 | 5 | 9 | 885 1991 LANCET 338(8772):956-957 HIRST M; KNIGHT S; DAVIES K; CROSS G; OCRAFT K; et al. PRENATAL-DIAGNOSIS OF FRAGILE-X SYNDROME | 29 | 35 |
| 886 | 4 | 6 | 886 1991 LANCET 338(8772):957-958 DOBKIN CS; DING XH; JENKINS EC; KRAWCZUN MS; BROWN WT; et al. PRENATAL-DIAGNOSIS OF FRAGILE-X SYNDROME | 22 | 24 |
| 887 | 0 | 0 | 887 1991 M S-MEDECINE SCIENCES 7(4):378-379 OBERLE I; MANDEL JL FRAGILE-X MENTAL-RETARDATION - VERY LOCALIZED GENOMIC IMPRINTING CLOSELY LINKED TO CLINICAL EXPRESSION | 0 | 0 |
| 888 | 0 | 0 | 888 1991 M S-MEDECINE SCIENCES 7(6):637-639 ROUSSEAU F; HEITZ D; OBERLE I; MANDEL JL; KRETZ C THE FRAGILE X-SYNDROME - NEW SURPRISES | 0 | 0 |
| 889 | 11 | 14 | 889 1991 NATURE 349(6310):624-626 VINCENT A; HEITZ D; PETIT C; KRETZ C; OBERLE I; et al. ABNORMAL PATTERN DETECTED IN FRAGILE-X PATIENTS BY PULSED-FIELD GEL-ELECTROPHORESIS | 112 | 165 |
| 890 | 3 | 12 | 890 1991 NATURE 349(6312):742-743 CRAIG I HUMAN-GENETICS - METHYLATION AND THE FRAGILE-X | 1 | 5 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 891 | 7 | 11 | 891 1991 NATURE 351(6326):439-440 DAVIES K HUMAN-GENETICS - BREAKING THE FRAGILE-X | 2 | 7 |
| 892 | 15 | 28 | 892 1991 NEW ENGLAND JOURNAL OF MEDICINE 325(24):1673-1681 ROUSSEAU F; HEITZ D; BIANCALANA V; BLUMENFELD S; KRETZ C; et al. DIRECT DIAGNOSIS BY DNA ANALYSIS OF THE FRAGILE X-SYNDROME OF MENTAL-RETARDATION | 290 | 445 |
| 893 | 6 | 11 | 893 1991 NEW ENGLAND JOURNAL OF MEDICINE 325(24):1720-1722 SUTHERLAND GR; GEDEON A; KORNMAN L; DONNELLY A; BYARD RW; et al. PRENATAL-DIAGNOSIS OF FRAGILE X-SYNDROME BY DIRECT DETECTION OF THE UNSTABLE DNA-SEQUENCE | 62 | 86 |
| 894 | 7 | 11 | 894 1991 NEW ENGLAND JOURNAL OF MEDICINE 325(24):1736-1738 SHAPIRO LR THE FRAGILE X-SYNDROME - A PECULIAR PATTERN OF INHERITANCE | 2 | 5 |
| 895 | 10 | 25 | 895 1991 NUCLEIC ACIDS RESEARCH 19(10):2567-2572 DIETRICH A; KIOSCHIS P; MONACO AP; GROSS B; KORN B; et al. MOLECULAR-CLONING AND ANALYSIS OF THE FRAGILE X-REGION IN MAN | 23 | 45 |
| 896 | 9 | 25 | 896 1991 NUCLEIC ACIDS RESEARCH 19(12):3283-3288 HIRST MC; RACK K; NAKAHORI Y; ROCHE A; BELL MV; et al. A YAC CONTIG ACROSS THE FRAGILE X SITE DEFINES THE REGION OF FRAGILITY | 16 | 42 |
| 897 | 10 | 20 | 897 1991 NUCLEIC ACIDS RESEARCH 19(16):4355-4359 NAKAHORI Y; KNIGHT SJL; HOLLAND J; SCHWARTZ C; ROCHE A; et al. MOLECULAR HETEROGENEITY OF THE FRAGILE-X SYNDROME | 61 | 91 |
| 898 | 0 | 0 | 898 1991 OPTOMETRY AND VISION SCIENCE 68(8):634-640 MAINO DM; WESSON M; SCHLANGE D; CIBIS G; MAINO JH OPTOMETRIC FINDINGS IN THE FRAGILE X-SYNDROME | 5 | 9 |
| 899 | 0 | 0 | 899 1991 PEDIATRIC RESEARCH 29(4):A134-A134 SHAPIRO LR; EALLONARDO SJ; WILMOT PL OTHER FOLATE SENSITIVE FRAGILE SITE EXPRESSION AND THE FRAGILE-X SYNDROME | 0 | 0 |
| 900 | 11 | 23 | 900 1991 PRENATAL DIAGNOSIS 11(5):333-338 WEBB T EXPRESSION OF FRAGILE-X IN A FEMALE FETUS DIAGNOSED AFTER CHORIONIC VILLUS SAMPLING | 3 | 4 |