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Nodes: 2369
Authors: 4634,
Journals: 373,
Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by LCS.
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| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 701 | 1 | 3 | 499 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):1-17 NERI G; OPITZ JM; MIKKELSEN M; JACOBS PA; DAVIES K; TURNER G CONFERENCE REPORT - 3RD INTERNATIONAL WORKSHOP ON THE FRAGILE-X AND X-LINKED MENTAL-RETARDATION | 6 | 15 |
| 702 | 5 | 22 | 514 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):115-121 WATSON MS; BREG WR; PAULS D; BROWN WT; CARROLL AJ; HOWARDPEEBLES PN; MERYASH D; SHAPIRO LR ANEUPLOIDY AND THE FRAGILE-X SYNDROME | 6 | 8 |
| 703 | 3 | 4 | 517 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):165-168 BUTLER MG; ALLEN GA; SINGH DN; CARPENTER NJ; HALL BD PHOTOANTHROPOMETRIC ANALYSIS OF INDIVIDUALS WITH THE FRAGILE-X SYNDROME | 6 | 10 |
| 704 | 3 | 3 | 532 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):417-422 TOMMERUP N; LAING S; CHRISTENSEN IJ; TURNER G SCREENING FOR THE FRAGILE-X - HOW MANY CELLS SHOULD WE ANALYZE | 6 | 8 |
| 705 | 3 | 4 | 543 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):625-631 SHERMAN SL; TURNER G; SHEFFIELD L; LAING S; ROBINSON H INVESTIGATION OF THE TWINNING RATE IN FAMILIES WITH THE FRAGILE-X SYNDROME | 6 | 8 |
| 706 | 4 | 30 | 587 1988 HUMAN GENETICS 79(4):292-296 LI SY; TSAI CC; CHOU MY; LIN JK A CYTOGENETIC STUDY OF MENTALLY-RETARDED SCHOOL-CHILDREN IN TAIWAN WITH SPECIAL REFERENCE TO THE FRAGILE X-CHROMOSOME | 6 | 17 |
| 707 | 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 |
| 708 | 9 | 21 | 705 1990 HUMAN GENETICS 85(6):590-594 YU WD; WENGER SL; STEELE MW X-CHROMOSOME IMPRINTING IN FRAGILE-X SYNDROME | 6 | 15 |
| 709 | 7 | 34 | 732 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 |
| 710 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 711 | 9 | 24 | 862 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 |
| 712 | 0 | 0 | 868 1991 JOURNAL OF MEDICAL GENETICS 28(12):809-810 JACOBS PA THE FRAGILE-X SYNDROME | 6 | 10 |
| 713 | 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 |
| 714 | 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 |
| 715 | 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 |
| 716 | 38 | 84 | 1090 1993 GENETIC COUNSELING 4(4):245-263 MAES B; FRYNS JP; VANWALLEGHEM M; VANDENBERGHE H FRAGILE-X SYNDROME AND AUTISM - A PREVALENT ASSOCIATION OR A MISINTERPRETED CONNECTION | 6 | 13 |
| 717 | 1 | 1 | 1140 1993 NATURE GENETICS 5(3):312-312 HINDS HL; ASHLEY CT; SUTCLIFFE JS; NELSON DL; WARREN ST; HOUSMAN DE; SCHALLING M TISSUE-SPECIFIC EXPRESSION OF FMR-1 PROVIDES EVIDENCE FOR A FUNCTIONAL-ROLE IN FRAGILE X-SYNDROME (VOL 3, PG 36, 1993) | 6 | 7 |
| 718 | 3 | 12 | 1142 1993 NEUROPEDIATRICS 24(4):211-213 REES M; DIEBOLD U; PARKER K; DOOSE H; GARDINER RM; WHITEHOUSE WP BENIGN CHILDHOOD EPILEPSY WITH CENTROTEMPORAL SPIKES AND THE FOCAL SHARP WAVE TRAIT IS NOT LINKED TO THE FRAGILE-X REGION | 6 | 23 |
| 719 | 11 | 27 | 1147 1993 SOMATIC CELL AND MOLECULAR GENETICS 19(4):393-404 LUO SY; ROBINSON JC; REISS AL; MIGEON BR DNA METHYLATION OF THE FRAGILE-X LOCUS IN SOMATIC AND GERM-CELLS DURING FETAL DEVELOPMENT - RELEVANCE TO THE FRAGILE-X SYNDROME AND X-INACTIVATION | 6 | 19 |
| 720 | 17 | 32 | 1156 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):309-314 CHIURAZZI P; DEGRAAFF E; NG J; VERKERK AJMH; WOLFSON S; FISCH GS; KOZAK L; NERI G; OOSTRA BA NO APPARENT INVOLVEMENT OF THE FMR1 GENE IN 5 PATIENTS WITH PHENOTYPIC MANIFESTATIONS OF THE FRAGILE-X-SYNDROME | 6 | 10 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 721 | 16 | 27 | 1233 1994 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 38:27-35 SABARATNAM M; LAVER S; BUTLER L; PEMBREY M FRAGILE-X SYNDROME IN NORTH-EAST ESSEX - TOWARDS SYSTEMATIC SCREENING - CLINICAL-SELECTION | 6 | 8 |
| 722 | 14 | 21 | 1297 1995 AMERICAN JOURNAL OF MEDICAL GENETICS 59(4):426-430 MCCONKIEROSELL A; ROBINSON H; WAKE S; STALEY LW; HELLER K; CRONISTER A DISSEMINATION OF GENETIC RISK INFORMATION TO RELATIVES IN THE FRAGILE-X SYNDROME - GUIDELINES FOR GENETIC COUNSELORS | 6 | 7 |
| 723 | 12 | 24 | 1302 1995 AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY 172(4):1236-1239 RYYNANEN M; KIRKINEN P; MANNERMAA A; SAARIKOSKI S CARRIER DIAGNOSIS OF THE FRAGILE-X SYNDROME - A CHALLENGE IN ANTENATAL CLINICS | 6 | 8 |
| 724 | 16 | 40 | 1373 1995 JOURNAL OF MEDICAL GENETICS 32(10):764-769 DEVRIES BBA; ROBINSON H; STOLTEDIJKSTRA I; GI CVTP; DIJKSTRA PF; VANDOOM J; HALLEY DJJ; OOSTRA BA; TURNER G; NIERMEIJER MF GENERAL OVERGROWTH IN THE FRAGILE-X SYNDROME - VARIABILITY IN THE PHENOTYPIC-EXPRESSION OF THE FMR1 GENE MUTATION | 6 | 15 |
| 725 | 6 | 13 | 1395 1996 AMERICAN JOURNAL OF HUMAN GENETICS 58(3):641-643 Brown WT; Zhong N; Dobkin C Positive fragile X microsatellite associations point to a common mechanism of dynamic mutation evolution | 6 | 12 |
| 726 | 11 | 28 | 1450 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 67(1):77-80 Simon EW; Finucane BM Facial emotion identification in males with fragile X syndrome | 6 | 6 |
| 727 | 37 | 74 | 1469 1996 COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY 61:679-687 Eberhart DE; Warren ST The molecular basis of fragile X syndrome | 6 | 8 |
| 728 | 12 | 14 | 1506 1996 PEDIATRIC NEUROLOGY 15(4):358-360 Kluger G; Bohm I; Laub MC; Waldenmaier C Epilepsy and fragile X gene mutations | 6 | 12 |
| 729 | 17 | 35 | 1515 1996 SOMATIC CELL AND MOLECULAR GENETICS 22(6):435-441 Eberhart DE; Warren ST Nuclease sensitivity of permeabilized cells confirms altered chromatin formation at the fragile X locus | 6 | 14 |
| 730 | 26 | 38 | 1597 1997 HUMAN MUTATION 10(5):393-399 Wang YC; Lin ML; Lin SJ; Li YC; Li SY Novel point mutation within intron 10 of FMR-1 gene causing fragile X syndrome | 6 | 9 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 731 | 27 | 57 | 1601 1997 JOURNAL OF INHERITED METABOLIC DISEASE 20(2):139-151 Hoogeveen AT; Oostra BA The fragile X syndrome | 6 | 10 |
| 732 | 20 | 34 | 1745 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):191-194 Zhong N; Ju WN; Xu WM; Ye LL; Shen Y; Wu GY; Chen SH; Jin RM; Hu XF; Yang AD; Liu XX; Poon P; Pang C; Zheng Y; Song L; Zhao P; Fu BJ; Gu HJ; Brown WT Frequency of the fragile X syndrome in Chinese mentally retarded populations is similar to that in Caucasians | 6 | 10 |
| 733 | 20 | 43 | 1812 1999 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 38(10):1294-1301 Murphy DGM; Mentis MJ; Pietrini P; Grady CL; Moore CJ; Horwitz B; Hinton V; Dobkin CS; Schapiro MB; Rapoport SI Premutation female carriers of fragile X syndrome: A pilot study on brain anatomy and metabolism | 6 | 7 |
| 734 | 10 | 14 | 1856 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 95(2):105-107 Tuncbilek E; Alikasifoglu M; Aktas D; Duman F; Yanik H; Anar B; Oostra B; Willemsen R Screening for the fragile X syndrome among mentally retarded males by hair root analysis | 6 | 6 |
| 735 | 8 | 32 | 1948 2000 MOLECULAR BRAIN RESEARCH 75(2):337-341 Valentine G; Chakravarty S; Sarvey J; Bramham C; Herkenham M Fragile X (fmr1) mRNA expression is differentially regulated in two adult models of activity-dependent gene expression | 6 | 9 |
| 736 | 37 | 73 | 2010 2001 COGNITIVE NEUROPSYCHOLOGY 18(1):1-18 Simon JA; Keenan JM; Pennington BF; Taylor AK; Hagerman RJ Discourse processing in women with fragile X syndrome: Evidence for a deficit establishing coherence | 6 | 7 |
| 737 | 7 | 25 | 2025 2001 HUMAN REPRODUCTION 16(3):457-462 Hundscheid RDL; Braat DDM; Kiemeney LALM; Smits APT; Thomas CMG Increased serum FSH in female fragile X premutation carriers with either regular menstrual cycles or on oral contraceptives | 6 | 10 |
| 738 | 19 | 31 | 2026 2001 INFANTS AND YOUNG CHILDREN 14(1):24-33 Bailey DB; Roberts JE; Mirrett P; Hatton DD Identifying infants and toddlers with fragile X syndrome: Issues and recommendations | 6 | 6 |
| 739 | 35 | 51 | 2116 2002 CURRENT OPINION IN GENETICS & DEVELOPMENT 12(3):278-283 Hagerman RJ; Hagerman PJ The fragile X premutation: into the phenotypic fold | 6 | 17 |
| 740 | 15 | 43 | 2170 2002 MOLECULAR AND CELLULAR BIOLOGY 22(23):8332-8341 Otero YD; Severijnen LA; van Cappellen G; Schrier M; Oostra B; Willemsen R Transport of fragile X mental retardation protein via granules in neurites of PC12 cells | 6 | 15 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 741 | 27 | 41 | 2196 2002 RNA-A PUBLICATION OF THE RNA SOCIETY 8(12):1482-1488 Primerano B; Tassone F; Hagerman RJ; Hagerman P; Amaldi F; Bagni C Reduced FMR1 mRNA translation efficiency in Fragile X patients with premutations | 6 | 10 |
| 742 | 13 | 15 | 2198 2002 TRENDS IN MOLECULAR MEDICINE 8(3):102-103 Oostra BA Functions of the fragile X protein | 6 | 8 |
| 743 | 13 | 30 | 2242 2003 ARCHIVES OF NEUROLOGY 60(1):117-121 Leehey MA; Munhoz RP; Lang AE; Brunberg JA; Grigsby J; Greco C; Jacquemont S; Tassone F; Lozano AM; Hagerman PJ; Hagerman RJ The fragile X premutation presenting as essential tremor | 6 | 13 |
| 744 | 1 | 15 | 34 1981 PEDIATRICS 68(4):594-595 GERALD PS X-LINKED MENTAL-RETARDATION AND THE FRAGILE-X SYNDROME | 5 | 11 |
| 745 | 0 | 0 | 41 1982 AMERICAN JOURNAL OF HUMAN GENETICS 34(6):A110-A110 SHAPIRO LR; HASEN J; GORDON G; SOUTHREN AL; WILMOT PL; BRENHOLZ P TESTICULAR INSUFFICIENCY AND DISORDERED THYROID METABOLISM IN THE FRAGILE X-CHROMOSOME SYNDROME | 5 | 7 |
| 746 | 0 | 5 | 59 1982 HUMAN GENETICS 60(1):80-81 ZANKL H; EBERLE G METHODS OF INCREASING THE VISIBILITY OF FRAGILE-X CHROMOSOMES | 5 | 8 |
| 747 | 0 | 1 | 148 1983 JOURNAL OF MEDICAL GENETICS 20(6):476-476 MORICPETROVIC S; LACA Z A FATHER AND DAUGHTER WITH FRAGILE X-CHROMOSOME | 5 | 7 |
| 748 | 0 | 4 | 151 1983 LANCET 2(8364):1427-1427 KINNELL HG; BANU SP INSTITUTIONAL PREVALENCE OF FRAGILE X-SYNDROME | 5 | 8 |
| 749 | 6 | 36 | 188 1984 AMERICAN JOURNAL OF MEDICINE 77(4):602-611 BRANDA RF; ARTHUR DC; WOODS WG; DANZL TJ; KING RA FOLATE METABOLISM AND CHROMOSOMAL STABILITY IN THE FRAGILE-X SYNDROME | 5 | 14 |
| 750 | 1 | 9 | 192 1984 CLINICAL GENETICS 25(2):135-139 GARDINER GB; WENGER SL; STEELE MW INVITRO REVERSAL OF FRAGILE-X EXPRESSION BY EXOGENOUS THYMIDINE | 5 | 7 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 751 | 6 | 16 | 231 1984 PRENATAL DIAGNOSIS 4(1):61-66 WILSON MG; MARCHESE CA PRENATAL-DIAGNOSIS OF FRAGILE-X IN A HETEROZYGOUS FEMALE FETUS AND POSTNATAL FOLLOW-UP | 5 | 9 |
| 752 | 4 | 8 | 264 1985 CLINICAL GENETICS 27(5):520-521 WEBB GC DETECTION OF THE FRAGILE X-CHROMOSOME AND OTHER FRAGILE SITES | 5 | 6 |
| 753 | 13 | 28 | 284 1985 HUMAN GENETICS 69(3):218-223 VONKOSKULL H; AULA P; AMMALA P; NORDSTROM AM; RAPOLA J IMPROVED TECHNIQUE FOR THE EXPRESSION OF FRAGILE-X IN CULTURED AMNIOTIC-FLUID CELLS | 5 | 9 |
| 754 | 2 | 7 | 308 1985 PRENATAL DIAGNOSIS 5(3):229-231 ROCCHI M; PECILE V; ARCHIDIACONO N; MONNI G; DUMEZ Y; FILIPPI G PRENATAL-DIAGNOSIS OF THE FRAGILE-X IN MALE MONOZYGOTIC TWINS - DISCORDANT EXPRESSION OF THE FRAGILE SITE IN AMNIOCYTES | 5 | 10 |
| 755 | 1 | 14 | 339 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):445-455 LEDBETTER DH; AIRHART SD; NUSSBAUM RL CAFFEINE ENHANCES FRAGILE-(X) EXPRESSION IN SOMATIC-CELL HYBRIDS | 5 | 18 |
| 756 | 8 | 16 | 340 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):467-473 KRAWCZUN MS; LELE KP; JENKINS EC; BROWN WT FRAGILE-X EXPRESSION INCREASED BY LOW CELL-CULTURE DENSITY | 5 | 8 |
| 757 | 8 | 18 | 390 1986 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 7(4):253-256 MADISON LS; WELLS TE; FRISTO TE; BENESCH CG A CONTROLLED-STUDY OF FOLIC-ACID TREATMENT IN 3 FRAGILE-X SYNDROME MALES | 5 | 6 |
| 758 | 8 | 19 | 414 1987 AMERICAN JOURNAL OF MEDICAL GENETICS 26(4):909-914 WENGER SL; HENNESSEY JC; STEELE MW INCREASED SISTER CHROMATID EXCHANGE FREQUENCY AT XQ27-SITE IN AFFECTED FRAGILE-X MALES | 5 | 23 |
| 759 | 7 | 17 | 419 1987 AMERICAN JOURNAL OF MEDICAL GENETICS 28(1):13-15 CHUDLEY AE; DEVONFLINDT R; HAGERMAN RJ COGNITIVE VARIABILITY IN THE FRAGILE X-SYNDROME | 5 | 9 |
| 760 | 13 | 30 | 424 1987 ARCHIVES OF OPHTHALMOLOGY 105(8):1099-1102 STORM RL; PEBENITO R; FERRETTI C OPHTHALMOLOGIC FINDINGS IN THE FRAGILE X-SYNDROME | 5 | 7 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 761 | 6 | 34 | 429 1987 BIOLOGICAL PSYCHIATRY 22(3):303-312 STCLAIR DM; BLACKWOOD DHR; OLIVER CJ; DICKENS P P3 ABNORMALITY IN FRAGILE-X SYNDROME | 5 | 16 |
| 762 | 2 | 4 | 430 1987 BRITISH JOURNAL OF PSYCHIATRY 150:700-702 DEB S; COWIE VA; TIMBERLAKE C A CASE OF MOSAICISM WITH FRAGILE-X AND FRAGILE-XXY COMPONENTS | 5 | 5 |
| 763 | 4 | 7 | 491 1987 PRENATAL DIAGNOSIS 7(3):197-202 SUTHERLAND GR; BAKER E; PURVISSMITH S; HOCKEY A; KRUMINS E; EICHENBAUM SZ PRENATAL-DIAGNOSIS OF THE FRAGILE-X USING THYMIDINE INDUCTION | 5 | 13 |
| 764 | 8 | 20 | 511 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):83-98 WALDSTEIN G; HAGERMAN R AORTIC HYPOPLASIA AND CARDIAC VALVULAR ABNORMALITIES IN A BOY WITH FRAGILE-X SYNDROME | 5 | 5 |
| 765 | 4 | 5 | 544 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):633-639 SHERMAN SL; TURNER G; ROBINSON H; LAING S INVESTIGATION OF THE SEGREGATION OF THE FRAGILE-X MUTATION IN DAUGHTERS OF OBLIGATE CARRIER WOMEN | 5 | 7 |
| 766 | 7 | 21 | 549 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):681-688 WARREN ST FRAGILE-X SYNDROME - A HYPOTHESIS REGARDING THE MOLECULAR MECHANISM OF THE PHENOTYPE | 5 | 6 |
| 767 | 1 | 13 | 571 1988 CLINICAL GENETICS 33(5):349-355 MERYASH DL; ABUELO D COUNSELING NEEDS AND ATTITUDES TOWARD PRENATAL-DIAGNOSIS AND ABORTION IN FRAGILE-X FAMILIES | 5 | 17 |
| 768 | 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 |
| 769 | 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 |
| 770 | 3 | 10 | 721 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 771 | 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 |
| 772 | 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 |
| 773 | 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 |
| 774 | 6 | 28 | 865 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 | 15 |
| 775 | 4 | 4 | 867 1991 JOURNAL OF MEDICAL GENETICS 28(5):358-358 WEBB T; BUNDEY S PREVALENCE OF FRAGILE X-SYNDROME | 5 | 8 |
| 776 | 0 | 0 | 891 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 |
| 777 | 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 |
| 778 | 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 |
| 779 | 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 |
| 780 | 4 | 9 | 1064 1993 AMERICAN JOURNAL OF MEDICAL GENETICS 47(2):216-220 WIEGERS AM; CURFS LMG; VERMEER ELMH; FRYNS JP ADAPTIVE-BEHAVIOR IN THE FRAGILE X-SYNDROME - PROFILE AND DEVELOPMENT | 5 | 6 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 781 | 7 | 7 | 1078 1993 CLINICAL GENETICS 43(3):157-159 MORNET E; JOKIC M; BOGYO A; TEJADA I; DELUCHAT C; BOUE J; BOUE A AFFECTED SIBS WITH FRAGILE-X SYNDROME EXHIBIT AN AGE-DEPENDENT DECREASE IN THE SIZE OF THE FRAGILE-X FULL MUTATION | 5 | 8 |
| 782 | 14 | 31 | 1093 1993 HUMAN GENETICS 91(5):469-474 LOESCH DZ; SHEFFIELD LJ; HAY DA BETWEEN-GENERATION DIFFERENCES IN ASCERTAINMENT AND PENETRANCE - RELEVANCE TO GENETIC HYPOTHESES IN FRAGILE-X | 5 | 5 |
| 783 | 6 | 13 | 1144 1993 PEDIATRICS 91(4):714-715 CRABBE LS; BENSKY AS; HORNSTEIN L; SCHWARTZ DC CARDIOVASCULAR-ABNORMALITIES IN CHILDREN WITH FRAGILE-X SYNDROME | 5 | 7 |
| 784 | 15 | 19 | 1179 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):458-462 TURNER AM; ROBINSON H; WAKE S; LAING SJ; LEIGH D; TURNER G COUNSELING RISK FIGURES FOR FRAGILE-X CARRIER FEMALES OF VARYING BAND SIZES FOR USE IN PREDICTING THE LIKELIHOOD OF RETARDATION IN THEIR OFFSPRING | 5 | 8 |
| 785 | 0 | 3 | 1196 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 53(4):382-382 HOWARDPEEBLES PN; MADDALENA A; SPENCE WC; LEVINSON G; FALLON L; BICK DP; BLACK SH; SCHULMAN JD FRAGILE-X SCREENING - WHAT IS THE REAL ISSUE | 5 | 9 |
| 786 | 20 | 27 | 1292 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(6):1408-1413 LOESCH DZ; HUGGINS R; PETROVIC V; SLATER H EXPANSION OF THE CGG REPEAT IN FRAGILE-X IN THE FMR1 GENE DEPENDS ON THE SEX OF THE OFFSPRING | 5 | 12 |
| 787 | 9 | 28 | 1299 1995 AMERICAN JOURNAL OF MEDICAL GENETICS 60(1):39-43 SPINELLI M; ROCHA ACD; GIACHETI CM; RICHIERICOSTA A WORD-FINDING DIFFICULTIES, VERBAL PARAPHASIAS, AND VERBAL DYSPRAXIA IN 10 INDIVIDUALS WITH FRAGILE-X-SYNDROME | 5 | 5 |
| 788 | 26 | 39 | 1312 1995 BRAIN & DEVELOPMENT 17(5):317-321 NANBA E; KOHNO Y; MATSUDA A; YANO M; SATO C; HASHIMOTO K; KOEDA T; YOSHINO K; KIMURA M; MAEOKA Y; YAMAMOTO T; MAEGAKI Y; EDA I; TAKESHITA K NONRADIOACTIVE DNA DIAGNOSIS FOR THE FRAGILE-X SYNDROME IN MENTALLY-RETARDED JAPANESE MALES | 5 | 15 |
| 789 | 20 | 28 | 1356 1995 HUMAN GENETICS 96(5):577-584 ELALEEM AA; BOHM I; TEMTAMY S; ELAWADY M; AWADALLA M; SCHMIDTKE J; STUHRMANN M DIRECT MOLECULAR ANALYSIS OF THE FRAGILE-X SYNDROME IN A SAMPLE OF EGYPTIAN AND GERMAN PATIENTS USING NONRADIOACTIVE PCR AND SOUTHERN BLOT FOLLOWED BY CHEMILUMINESCENT DETECTION | 5 | 9 |
| 790 | 22 | 37 | 1364 1995 JOURNAL OF CLINICAL AND EXPERIMENTAL NEUROPSYCHOLOGY 17(4):518-528 HINTON VJ; HALPERIN JM; DOBKIN CS; DING XH; BROWN WT; MIEZEJESKI CM COGNITIVE AND MOLECULAR ASPECTS OF FRAGILE-X | 5 | 7 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 791 | 13 | 35 | 1375 1995 JOURNAL OF MEDICAL GENETICS 32(12):925-929 KIRCHGESSNER CU; WARREN ST; WILLARD HF X INACTIVATION OF THE FMR1 FRAGILE-X MENTAL-RETARDATION GENE | 5 | 12 |
| 792 | 27 | 61 | 1382 1995 NEUROPSYCHOLOGY 9(4):470-480 MAZZOCCO MMM; FREUND LS; BAUMGARDNER TL; FORMAN L; REISS AL NEUROPSYCHOLOGICAL AND PSYCHOSOCIAL EFFECTS OF THE FMR-1 FULL MUTATION - CASE-REPORT OF MONOZYGOTIC TWINS DISCORDANT FOR THE FRAGILE-X SYNDROME | 5 | 6 |
| 793 | 11 | 12 | 1408 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):176-180 Perroni L; Grasso M; Argusti A; LoNigro C; Croci GF; Zelante L; Garani GP; Bricarelli FD Molecular and cytogenetic analysis of the fragile X syndrome in a series of 453 mentally retarded subjects: A study of 87 families | 5 | 6 |
| 794 | 13 | 20 | 1417 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):234-238 Syrrou M; Patsalis PC; Georgiou I; Hadjimarcou MI; ConstantinouDeltas CD; Pagoulatos G Evidence for high-risk haplotypes and (CGG)n expansion in fragile X syndrome in the Hellenic population of Greece and Cyprus | 5 | 15 |
| 795 | 4 | 9 | 1430 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):319-322 Fisch GS; Carpenter N; Maddalena A; Tarleton J; JulienInalsingh C; Holden JJA Rater reliability of fragile X mutation size estimates: A multilaboratory analysis | 5 | 5 |
| 796 | 12 | 31 | 1431 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):323-328 Mazzocco MMM; Holden JJA Neuropsychological profiles of three sisters homozygous for the fragile X premutation | 5 | 7 |
| 797 | 3 | 11 | 1555 1997 AMERICAN JOURNAL OF MEDICAL GENETICS 69(1):114-116 Martin NG; Healey SC; Pangan TS; Heath AC; Turner G Do mothers of dizygotic twins have earlier menopause? A role for fragile X? | 5 | 12 |
| 798 | 6 | 10 | 1564 1997 ANNALS OF CLINICAL BIOCHEMISTRY 34:517-520 Chen TA; Lu XF; Che PK; Ho WKK Variation of the CGG repeat in FMR-1 gene in normal and fragile X Chinese subjects | 5 | 7 |
| 799 | 8 | 10 | 1574 1997 BRITISH MEDICAL JOURNAL 315(7117):1223-1226 Turner G; Robinson H; Wake S; Laing S; Partington M Case finding for the fragile X syndrome and its consequences | 5 | 9 |
| 800 | 14 | 19 | 1591 1997 HUMAN GENETICS 100(5-6):564-568 Larsen LA; Gronskov K; NorgaardPedersen B; BrondumNielsen K; Hasholt L; Vuust J High-throughput analysis of fragile X (CGG)(n) alleles in the normal and premutation range by PCR amplification and automated capillary electrophoresis | 5 | 23 |
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