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Nodes: 2369
Authors: 4634,
Journals: 373,
Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by year, source, volume, issue, page.
Page 7: 1 (1) 2 (101) 3 (201) 4 (301) 5 (401) 6 (501) 7 (601) 8 (701) 9 (801) 10 (901) 11 (1001) 12 (1101) 13 (1201) 14 (1301) 15 (1401) 16 (1501) 17 (1601) 18 (1701) 19 (1801) 20 (1901) 21 (2001) 22 (2101) 23 (2201) 24 (2301)
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 601 | 1 | 1 | 601 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 |
| 602 | 0 | 0 | 602 1988 JOURNAL OF MEDICAL GENETICS 25(2):128-128 ENGLISH C ANTHROPOMETRIC STUDIES IN THE FRAGILE X-SYNDROME | 0 | 0 |
| 603 | 0 | 0 | 603 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 |
| 604 | 0 | 0 | 604 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 |
| 605 | 5 | 17 | 605 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 |
| 606 | 0 | 0 | 606 1988 NEUROTOXICOLOGY 9(1):139-140 EDWARDS DR; KEPPEN LD; GOLLIN SM AUTISM AND FRAGILE-X SYNDROME | 0 | 0 |
| 607 | 5 | 9 | 607 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 |
| 608 | 27 | 63 | 608 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 |
| 609 | 3 | 31 | 609 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 |
| 610 | 0 | 0 | 610 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 611 | 0 | 0 | 611 1989 AMERICAN FAMILY PHYSICIAN 39(5):185-193 SIMENSEN RJ; ROGERS RC FRAGILE-X SYNDROME | 1 | 1 |
| 612 | 14 | 29 | 612 1989 AMERICAN JOURNAL OF HUMAN GENETICS 45(2):304-309 DAHL N; GOONEWARDENA P; MALMGREN H; GUSTAVSON KH; HOLMGREN G; SEEMANOVA E; ANNEREN G; FLOOD A; PETTERSSON U LINKAGE ANALYSIS OF FAMILIES WITH FRAGILE-X MENTAL-RETARDATION, USING A NOVEL RFLP MARKER (DXS 304) | 19 | 40 |
| 613 | 9 | 24 | 613 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 |
| 614 | 4 | 10 | 614 1989 AMERICAN JOURNAL OF HUMAN GENETICS 45(6):977-978 FERRI R BRAIN-STEM AUDITORY EVOKED-POTENTIALS IN THE FRAGILE-X SYNDROME | 2 | 3 |
| 615 | 2 | 7 | 615 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 |
| 616 | 7 | 18 | 616 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 |
| 617 | 5 | 19 | 617 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 |
| 618 | 11 | 30 | 618 1989 AMERICAN JOURNAL OF MEDICAL GENETICS 33(4):513-518 HAGERMAN RJ; SCHREINER RA; KEMPER MB; WITTENBERGER MD; ZAHN B; HABICHT K LONGITUDINAL IQ CHANGES IN FRAGILE-X MALES | 34 | 46 |
| 619 | 21 | 44 | 619 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 |
| 620 | 10 | 14 | 620 1989 AMERICAN JOURNAL OF MEDICAL GENETICS 34(2):302-303 COHEN IL; BROWN WT; JENKINS EC; KRAWCZUN MS; FRENCH JH; RAGUTHU S; WOLFSCHEIN EG; SUDHALTER V; FISCH G; WISNIEWSKI K FRAGILE-X SYNDROME IN FEMALES WITH AUTISM | 13 | 16 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 621 | 30 | 58 | 621 1989 AMERICAN JOURNAL OF ORTHOPSYCHIATRY 59(1):142-152 HAGERMAN RJ; SOBESKY WE PSYCHOPATHOLOGY IN FRAGILE-X-SYNDROME | 28 | 40 |
| 622 | 0 | 0 | 622 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 |
| 623 | 11 | 24 | 623 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 | 25 | 38 |
| 624 | 4 | 53 | 624 1989 AMERICAN ZOOLOGIST 29(2):569-591 LAIRD CD FROM POLYTENE CHROMOSOMES TO HUMAN EMBRYOLOGY - CONNECTIONS VIA THE HUMAN FRAGILE-X SYNDROME | 1 | 3 |
| 625 | 38 | 83 | 625 1989 ARCHIVES FRANCAISES DE PEDIATRIE 46(3):211-216 LELOUARN P; MORAINE C; PERROT A; BARTHELEMY C; GARREAU B; SAUVAGE D AUTISM AND FRAGILE X-SYNDROME | 3 | 5 |
| 626 | 6 | 8 | 626 1989 ARCHIVES OF DISEASE IN CHILDHOOD 64(9):1223-1224 WINTER RM FRAGILE-X MENTAL-RETARDATION | 1 | 3 |
| 627 | 2 | 17 | 627 1989 ARCHIVES OF NEUROLOGY 46(12):1269-1270 GRIGSBY J; HAGERMAN R FRAGILE-X SYNDROME - A GENETIC ETIOLOGY FOR DEVELOPMENTAL GERSTMANN SYNDROME | 0 | 0 |
| 628 | 4 | 9 | 628 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 |
| 629 | 2 | 31 | 629 1989 CLINICAL GENETICS 36(1):15-24 MERYASH DL PERCEPTION OF BURDEN AMONG AT-RISK WOMEN OF RAISING A CHILD WITH FRAGILE-X SYNDROME | 2 | 7 |
| 630 | 9 | 14 | 630 1989 CLINICAL GENETICS 36(1):25-30 TUCKERMAN E; WEBB T THE INACTIVATION OF THE FRAGILE X-CHROMOSOME IN FEMALE CARRIERS OF THE MARTIN-BELL SYNDROME AS STUDIED BY 2 DIFFERENT METHODS | 4 | 6 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 631 | 0 | 0 | 631 1989 CLINICAL RESEARCH 37(1):A170-A170 HAGERMAN RJ; SCHREINER RA; KEMPER MB; WITTENBERGER MD; ZAHN B; HABICHT K LONGITUDINAL IQ CHANGES IN FRAGILE-X MALES | 0 | 0 |
| 632 | 2 | 10 | 632 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 |
| 633 | 0 | 0 | 633 1989 CYTOGENETICS AND CELL GENETICS 51(1-4):982-982 DAHL N; MALMSTROM H; HAMMARSTROMHEEROMA K; WADELIUS C; GUSTAVSON KH; HOLMGREN G; PETTERSSON U ISOLATION OF A NEW DNA MARKER TIGHTLY LINKED TO THE FRAGILE-X LOCUS (FRAXA) | 0 | 3 |
| 634 | 0 | 0 | 634 1989 CYTOGENETICS AND CELL GENETICS 51(1-4):1007-1007 GOONEWARDENA P; GROSS AC; FERRANDO CJ; BROWN T; DAHL N; PETTERSSON U 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 |
| 635 | 0 | 0 | 635 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 |
| 636 | 0 | 0 | 636 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 |
| 637 | 0 | 0 | 637 1989 CYTOGENETICS AND CELL GENETICS 51(1-4):1089-1090 THIBODEAU SN; SCHAID D; BREN G; BLOOMFIELD J; BELL MV; SCHWARTZ CE; HAGERMAN R; DAVIES KE GENETIC-MAPPING OF A NOVEL REGION CLOSE TO THE FRAGILE X-SITE ON THE HUMAN X-CHROMOSOME | 0 | 1 |
| 638 | 0 | 1 | 638 1989 CYTOGENETICS AND CELL GENETICS 51(1-4):1100-1101 WAHLSTROM J; WITTENGERSTROM I; ANVRET M; ODEN A; JOHANNESSON T; HOLMQUIST D RETT SYNDROME RELATED TO FRAGILE X(P22) IN CAFFEINE-INDUCED LYMPHOCYTES CULTURES | 0 | 2 |
| 639 | 0 | 0 | 639 1989 GENOMICS 4(4):570-578 PATTERSON MN; BELL MV; BLOOMFIELD J; FLINT T; DORKINS H; THIBODEAU SN; SCHAID D; BREN G; SCHWARTZ CE; WIERINGA B; ROPERS HH; CALLEN DF; SUTHERLAND G; FROSTERISKENIUS U; VISSING H; DAVIES KE GENETIC AND PHYSICAL MAPPING OF A NOVEL REGION CLOSE TO THE FRAGILE X-SITE ON THE HUMAN X-CHROMOSOME | 17 | 43 |
| 640 | 0 | 0 | 640 1989 GENOMICS 5(4):797-801 VINCENT A; DAHL N; OBERLE I; HANAUER A; MANDEL JL; MALMGREN H; PETTERSSON U THE POLYMORPHIC MARKER DXS304 IS WITHIN 5-CENTIMORGANS OF THE FRAGILE-X LOCUS | 13 | 23 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 641 | 4 | 22 | 641 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 |
| 642 | 10 | 17 | 642 1989 HUMAN GENETICS 82(1):79-81 SCHAAP T THE ROLE OF RECOMBINATION IN THE EVOLVEMENT OF THE FRAGILE X-MUTATION | 2 | 2 |
| 643 | 7 | 16 | 643 1989 HUMAN GENETICS 82(3):216-218 DAHL N; HAMMARSTROMHEEROMA K; GOONEWARDENA P; WADELIUS C; GUSTAVSON KH; HOLMGREN G; VANOMMEN GJB; PETTERSSON U ISOLATION OF A DNA PROBE OF POTENTIAL USE FOR DIAGNOSIS OF THE FRAGILE-X SYNDROME | 17 | 32 |
| 644 | 9 | 19 | 644 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 |
| 645 | 6 | 7 | 645 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 |
| 646 | 0 | 1 | 646 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 |
| 647 | 2 | 33 | 647 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 | 30 | 47 |
| 648 | 4 | 9 | 648 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 |
| 649 | 10 | 16 | 649 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 |
| 650 | 5 | 34 | 650 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; LECKMAN JF THE TRAJECTORY OF DEVELOPMENT IN MALES WITH FRAGILE-X SYNDROME | 31 | 50 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 651 | 9 | 27 | 651 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 | 16 | 27 |
| 652 | 4 | 4 | 652 1989 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 28(6):965-966 FISCH GS FRAGILE-X AND AUTISM | 3 | 4 |
| 653 | 3 | 4 | 653 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 |
| 654 | 1 | 5 | 654 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 |
| 655 | 0 | 0 | 655 1989 M S-MEDECINE SCIENCES 5(7):450-458 JORDAN BR; MATTEI JF FRAGILE X-LINKED MENTAL-RETARDATION, 1989 | 2 | 2 |
| 656 | 0 | 1 | 656 1989 NATURE 341(6243):580-580 HARRIS A; BOBROW M THE FRAGILE-X SYNDROME - DAVIES,KE | 0 | 0 |
| 657 | 0 | 0 | 657 1989 NEUROLOGIC CLINICS 7(1):107-121 BROWN WT THE FRAGILE-X SYNDROME | 1 | 1 |
| 658 | 0 | 0 | 658 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 |
| 659 | 8 | 19 | 659 1989 PEDIATRICS 83(4):547-552 SIMKO A; HORNSTEIN L; SOUKUP S; BAGAMERY N FRAGILE X-SYNDROME - RECOGNITION IN YOUNG-CHILDREN | 28 | 31 |
| 660 | 3 | 3 | 660 1989 PRENATAL DIAGNOSIS 9(11):777-781 WEBB TP; BUNDEY S; MCKINLEY M MISSED PRENATAL-DIAGNOSIS OF FRAGILE-X SYNDROME | 3 | 5 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 661 | 21 | 41 | 661 1989 PSYCHOLOGY IN THE SCHOOLS 26(4):380-389 SIMENSEN RJ; ROGERS RC SCHOOL-PSYCHOLOGY AND MEDICAL DIAGNOSIS - THE FRAGILE X-SYNDROME | 1 | 1 |
| 662 | 0 | 0 | 662 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 |
| 663 | 0 | 3 | 663 1989 SCIENCE 243(4888):171-172 BARNES DM FRAGILE-X SYNDROME AND ITS PUZZLING GENETICS | 3 | 9 |
| 664 | 4 | 22 | 664 1989 SCIENCE 246(4935):1298-1300 SUTHERS GK; CALLEN DF; HYLAND VJ; KOZMAN HM; BAKER E; EYRE H; HARPER PS; ROBERTS SH; HORSCAYLA MC; DAVIES KE; BELL MV; SUTHERLAND GR A NEW DNA MARKER TIGHTLY LINKED TO THE FRAGILE-X LOCUS (FRAXA) | 31 | 66 |
| 665 | 2 | 3 | 665 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 |
| 666 | 29 | 39 | 666 1989 ZEITSCHRIFT FUR KINDER-UND JUGENDPSYCHIATRIE UND PSYCHOTHERAPIE 17(2):91-97 VONGONTARD A PSYCHOPATHOLOGY ASSOCIATED WITH THE FRAGILE-X SYNDROME | 1 | 2 |
| 667 | 0 | 0 | 667 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 |
| 668 | 5 | 14 | 668 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 |
| 669 | 19 | 66 | 669 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 |
| 670 | 12 | 33 | 670 1990 AMERICAN JOURNAL OF HUMAN GENETICS 46(4):738-743 ROCCHI M; ARCHIDIACONO N; RINALDI A; FILIPPI G; BARTOLUCCI G; FANCELLO GS; SINISCALCO M MENTAL-RETARDATION IN HETEROZYGOTES FOR THE FRAGILE-X MUTATION - EVIDENCE IN FAVOR OF AN X INACTIVATION-DEPENDENT EFFECT | 11 | 13 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 671 | 11 | 44 | 671 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 |
| 672 | 18 | 37 | 672 1990 AMERICAN JOURNAL OF HUMAN GENETICS 47(2):175-180 BROWN WT INVITED EDITORIAL - THE FRAGILE-X - PROGRESS TOWARD SOLVING THE PUZZLE | 28 | 41 |
| 673 | 6 | 24 | 673 1990 AMERICAN JOURNAL OF HUMAN GENETICS 47(2):181-187 MACKINNON RN; HIRST MC; BELL MV; WATSON JEV; CLAUSSEN U; LUDECKE HJ; SENGER G; HORSTHEMKE B; DAVIES KE MICRODISSECTION OF THE FRAGILE-X REGION | 9 | 37 |
| 674 | 6 | 38 | 674 1990 AMERICAN JOURNAL OF HUMAN GENETICS 47(2):187-195 SUTHERS GK; HYLAND VJ; CALLEN DF; OBERLE I; ROCCHI M; THOMAS NS; MORRIS CP; SCHWARTZ CE; SCHMIDT M; ROPERS HH; BAKER E; OOSTRA BA; DAHL N; WILSON PJ; HOPWOOD JJ; SUTHERLAND GR PHYSICAL MAPPING OF NEW DNA PROBES NEAR THE FRAGILE-X MUTATION (FRAXA) BY USING A PANEL OF CELL-LINES | 26 | 64 |
| 675 | 19 | 35 | 675 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 |
| 676 | 12 | 20 | 676 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 |
| 677 | 19 | 43 | 677 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 |
| 678 | 7 | 30 | 678 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 | 22 | 28 |
| 679 | 9 | 16 | 679 1990 AMERICAN JOURNAL OF MEDICAL GENETICS 36(1):122-125 VANROY BC; WILLEMS PJ; VITS LJ; CEULEMANS BP; COUCKE PJ; VANDERAUWERA BJ; LORMANS JAG; DUMON JE 2 BROTHERS WITH MENTAL-RETARDATION DISCORDANT FOR THE FRAGILE-X SYNDROME | 3 | 4 |
| 680 | 6 | 17 | 680 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 681 | 1 | 2 | 681 1990 AMERICAN JOURNAL OF MEDICAL GENETICS 37(3):433-433 MEISNER LF FRAGILE-X FREQUENCY | 0 | 0 |
| 682 | 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 |
| 683 | 2 | 6 | 683 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 |
| 684 | 11 | 23 | 684 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 | 51 | 64 |
| 685 | 9 | 32 | 685 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 |
| 686 | 8 | 13 | 686 1990 ANNALES DE GENETIQUE 33(2):109-110 LUCOTTE G A NEW DNA PROBE OF POTENTIAL USE FOR DIAGNOSIS OF THE FRAGILE-X SYNDROME | 0 | 0 |
| 687 | 0 | 0 | 687 1990 ANNALS OF NEUROLOGY 28(3):440-440 BERRYKRAVIS E; HUTTENLOCHER PR CYCLIC-AMP METABOLISM IN FRAGILE X-SYNDROME | 0 | 0 |
| 688 | 1 | 40 | 688 1990 ARCHIVES FRANCAISES DE PEDIATRIE 47(10):701-703 PIUSSAN C X-LINKED MENTAL-RETARDATION WITHOUT FRAGILE X-CHROMOSOME | 0 | 0 |
| 689 | 2 | 4 | 689 1990 ARCHIVES OF DISEASE IN CHILDHOOD 65(3):335-335 REDINGTON A; BUSH A FRAGILE-X MENTAL-RETARDATION | 2 | 2 |
| 690 | 28 | 73 | 690 1990 BIOLOGICAL PSYCHIATRY 27(2):223-240 REISS AL; FREUND L FRAGILE X-SYNDROME | 22 | 28 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 691 | 1 | 14 | 691 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 |
| 692 | 2 | 14 | 692 1990 BRITISH DENTAL JOURNAL 168(4):160-162 NUNN JH; DURNING P FRAGILE-X (MARTIN BELL) SYNDROME AND DENTAL-CARE | 0 | 0 |
| 693 | 6 | 13 | 693 1990 BRITISH JOURNAL OF HOSPITAL MEDICINE 43(1):17-17 BUNDEY S FRAGILE-X SYNDROME | 1 | 1 |
| 694 | 24 | 44 | 694 1990 CLINICAL GENETICS 37(1):2-11 SUTHERLAND GR; MULLEY JC DIAGNOSTIC MOLECULAR-GENETICS OF THE FRAGILE-X | 14 | 16 |
| 695 | 5 | 23 | 695 1990 CLINICAL GENETICS 37(3):167-172 SUTHERLAND GR; BAKER E THE COMMON FRAGILE SITE IN BAND Q27 OF THE HUMAN X-CHROMOSOME IS NOT COINCIDENT WITH THE FRAGILE-X | 29 | 43 |
| 696 | 13 | 27 | 696 1990 CLINICAL GENETICS 37(5):341-346 BORGHGRAEF M; FRYNS JP; VANDENBERGHE H THE FEMALE AND THE FRAGILE X-SYNDROME - DATA ON CLINICAL AND PSYCHOLOGICAL FINDINGS IN 7 FRA(X) CARRIERS | 16 | 20 |
| 697 | 0 | 0 | 697 1990 CLINICAL RESEARCH 38(1):A164-A164 HAGERMAN R; AMIRI K; CRONISTER A; WITTENBERGER M; SCHREINER R; SOBESKY W FRAGILE-X GIRLS - PHYSICAL AND NEUROCOGNITIVE STATUS AND OUTCOME | 0 | 0 |
| 698 | 1 | 12 | 698 1990 CYTOMETRY 11(1):73-79 PIPER J; FANTES J; GOSDEN J; JI L AUTOMATIC DETECTION OF FRAGILE X-CHROMOSOMES USING AN X-CENTROMERE PROBE | 0 | 4 |
| 699 | 10 | 27 | 699 1990 EUROPEAN NEUROLOGY 30(1):32-37 RAIMONDI E; LENTI C; ROMAGNONI M; NEGRI R; GAMBINI E; MUSETTI L; DECARLI L FRAGILE-X MENTAL-RETARDATION IN A LARGE 5-GENERATION FAMILY - A CLINICAL AND CYTOGENETIC STUDY | 0 | 0 |
| 700 | 6 | 12 | 700 1990 HUMAN GENETICS 84(2):216-217 BUTLER MG NO SIGNIFICANT RELATIONSHIP BETWEEN AGE AND FREQUENCY OF CHROMOSOME LESIONS IN MENTALLY-RETARDED INDIVIDUALS WITH OR WITHOUT THE FRAGILE X-SYNDROME | 1 | 4 |
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