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Nodes: 2369
Authors: 4634,
Journals: 373,
Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by GCS.
Page 11: 1 (1246) 2 (77) 3 (47) 4 (34) 5 (25) 6 (19) 7 (14) 8 (11) 9 (9) 10 (7) 11 (5) 12 (4) 13 (3) 14 (2) 15 (1) 16 (1) 17 (0) 18 (0) 19 (0) 20 (0) 21 (0) 22 (0) 23 (0) 24 (0)
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 1001 | 8 | 14 | 452 1987 HUMAN GENETICS 75(3):294-295 BROWN WT; SHERMAN SL; DOBKIN CS HYPOTHESIS REGARDING THE NATURE OF THE FRAGILE-X MUTATION - A REPLY | 3 | 5 |
| 1002 | 1 | 2 | 483 1987 LANCET 2(8554):329-329 VERLOES A; SACRE JP; GEUBELLE F SOTOS SYNDROME AND FRAGILE-X CHROMOSOMES | 1 | 5 |
| 1003 | 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 |
| 1004 | 1 | 2 | 533 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):423-428 TURNER G; PARTINGTON MW FRAGILE(X) EXPRESSION, AGE AND THE DEGREE OF INTELLECTUAL HANDICAP IN THE MALE | 4 | 5 |
| 1005 | 4 | 44 | 566 1988 BRAIN AND LANGUAGE 34(2):203-221 VILKMAN E; NIEMI J; IKONEN U FRAGILE-X SPEECH PHONOLOGY IN FINNISH | 4 | 5 |
| 1006 | 2 | 29 | 569 1988 CHROMOSOMA 97(1):6-10 KEREM B; GOITEIN R; SCHAAP T CYTOLOGICAL EVIDENCE OF DEFECTIVE TEMPLATE IN THE FRAGILE X-CHROMOSOME | 2 | 5 |
| 1007 | 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 |
| 1008 | 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 |
| 1009 | 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 |
| 1010 | 8 | 33 | 704 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 |
| 1011 | 0 | 0 | 709 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 |
| 1012 | 15 | 22 | 712 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 |
| 1013 | 12 | 22 | 811 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):421-424 ROSENBERG C; VIANNAMORGANTE AM; OTTO PA; NAVAJAS L EFFECT OF X-INACTIVATION ON FRAGILE-X FREQUENCY AND MENTAL-RETARDATION | 3 | 5 |
| 1014 | 1 | 15 | 832 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 |
| 1015 | 3 | 12 | 883 1991 NATURE 349(6312):742-743 CRAIG I HUMAN-GENETICS - METHYLATION AND THE FRAGILE-X | 1 | 5 |
| 1016 | 7 | 11 | 887 1991 NEW ENGLAND JOURNAL OF MEDICINE 325(24):1736-1738 SHAPIRO LR THE FRAGILE X-SYNDROME - A PECULIAR PATTERN OF INHERITANCE | 2 | 5 |
| 1017 | 1 | 16 | 920 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):124-127 TIROSH E; BOROCHOWITZ Z SLEEP-APNEA IN FRAGILE-X SYNDROME | 3 | 5 |
| 1018 | 4 | 14 | 957 1992 AMERICAN JOURNAL ON MENTAL RETARDATION 96(5):528-535 MERYASH DL CHARACTERISTICS OF FRAGILE-X RELATIVES WITH DIFFERENT ATTITUDES TOWARD TERMINATING AN AFFECTED PREGNANCY | 4 | 5 |
| 1019 | 18 | 33 | 1010 1992 PEDIATRIC NEUROLOGY 8(4):272-274 WONG VCN; LAM STS FRAGILE X POSITIVITY IN CHINESE CHILDREN WITH AUTISTIC SPECTRUM DISORDER | 3 | 5 |
| 1020 | 12 | 15 | 1063 1993 AMERICAN JOURNAL OF MEDICAL GENETICS 46(6):687-688 LAIRD CD IMPRINTING AND IMPRINT ERASURE AS VIEWED THROUGH THE FRAGILE-X SYNDROME | 2 | 5 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1021 | 1 | 8 | 1074 1993 BRITISH JOURNAL OF HAEMATOLOGY 85(2):415-416 VORST EJ; LEVENE NA; NISANI R; BERREBI A FRAGILE-X SYNDROME AND MYELODYSPLASIA DISCOVERED DURING PREGNANCY | 3 | 5 |
| 1022 | 16 | 20 | 1082 1993 CLINICAL GENETICS 44(4):169-172 YAMAUCHI M; NAGATA S; SEKI N; TOYAMA Y; HARADA N; NIIKAWA N; MASUNO I; KAJII T; HORI T PRENATAL-DIAGNOSIS OF FRAGILE X-SYNDROME BY DIRECT-DETECTION OF THE DYNAMIC MUTATION DUE TO AN UNSTABLE DNA-SEQUENCE | 2 | 5 |
| 1023 | 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 |
| 1024 | 17 | 34 | 1129 1993 MEDICAL JOURNAL OF AUSTRALIA 158(7):482-485 SUTHERLAND GR; MULLEY JC; RICHARDS RI FRAGILE-X SYNDROME - THE MOST COMMON CAUSE OF FAMILIAL INTELLECTUAL HANDICAP | 1 | 5 |
| 1025 | 4 | 8 | 1248 1994 MOLECULAR AND CELLULAR PROBES 8(2):177-180 CAO J; TARLETON J; BARBERIO D; DAVIDOW LS A SIMPLE FRAGILE-X PCR ASSAY WITH 7-DEAZAGUANINE-SUBSTITUTED DNA VISUALIZED BY ETHIDIUM-BROMIDE | 2 | 5 |
| 1026 | 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 |
| 1027 | 18 | 19 | 1300 1995 AMERICAN JOURNAL OF MEDICAL GENETICS 60(4):302-306 MUELLER OT; HARTSFIELD JK; AMAR MJA; GALLARDO LA; KOUSSEFF BG FRAGILE-X SYNDROME - DISCORDANT LEVELS OF CGG REPEAT MOSAICISM IN 2 BROTHERS | 2 | 5 |
| 1028 | 39 | 112 | 1309 1995 BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE 1271(2-3):293-303 FLANNERY AV; HIRST MC; KNIGHT SJL; RITCHIE RJ; DAVIES KE THE FRAGILE-X SYNDROME | 2 | 5 |
| 1029 | 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 |
| 1030 | 4 | 13 | 1458 1996 ARCHIVES OF MEDICAL RESEARCH 27(4):587-588 Rivera H Fragile X studies and authorship | 1 | 5 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1031 | 58 | 71 | 1476 1996 EUROPEAN PSYCHIATRY 11(5):233-243 Franke P; Barbe B; Leboyer M; Maier W Fragile X syndrome .2. Cognitive and behavioral correlates of mutations of the FMR-1 gene | 4 | 5 |
| 1032 | 8 | 27 | 1512 1996 PSYCHIATRY RESEARCH 64(2):97-104 Thompson NM; Rogeness GA; McClure E; Clayton R; Johnson C Influence of depression on cognitive functioning in Fragile X females | 1 | 5 |
| 1033 | 3 | 14 | 1554 1997 AMERICAN JOURNAL OF MEDICAL GENETICS 68(4):445-449 Wen GY; Jenkins EC; Yao XL; Yoon D; Brown WT; Wisniewski HM Transmission electron microscopy of chromosomes by longitudinal section preparation: Application to fragile X chromosome analysis | 3 | 5 |
| 1034 | 1 | 9 | 1576 1997 CLINICAL GENETICS 51(1):71-74 Behjati F; Mullarkey M; Bergbaum A; Berry AC; Docherty Z Chromosome deletion 17p11.2 (Smith-Magenis syndrome) in seven new patients, four of whom had been referred for fragile-X investigation | 0 | 5 |
| 1035 | 5 | 8 | 1588 1997 HOSPITAL PRACTICE 32(4):73-& Warren ST Trinucleotide repetition and fragile X syndrome | 3 | 5 |
| 1036 | 12 | 28 | 1642 1998 CLINICAL GENETICS 53(3):179-183 Chan SY; Wong V DNA diagnosis of FRAXA and FRAXE in Chinese children with neurodevelopmental disorders and fragile X syndrome | 2 | 5 |
| 1037 | 19 | 29 | 1662 1998 HUMAN HEREDITY 48(5):256-265 Hecimovic S; Barisic I; Pavelic K DNA analysis of the fragile X syndrome in an at risk pediatric population in Croatia: Simple clinical preselection criteria can considerably improve the cost-effectiveness of fragile X screening studies | 3 | 5 |
| 1038 | 2 | 4 | 1665 1998 HUMAN MUTATION 12(6):431-431 Vincent JB; Gurling HMD Point mutation in intron 10 of FMR1 is unlikely to be a cause of fragile X syndrome | 3 | 5 |
| 1039 | 14 | 23 | 1755 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):268-271 Zhong N; Ju W; Nelson D; Dobkin C; Brown WT Reduced mRNA for G3BP in fragile X cells: Evidence of FMR1 gene regulation | 3 | 5 |
| 1040 | 5 | 12 | 1763 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 87(4):366-368 Torrioli MG; Vernacotola S; Mariotti P; Bianchi E; Calvani M; De Gaetano A; Chiurazzi P; Neri G Double-blind, placebo-controlled study of L-acetylcarnitine for the treatment of hyperactive behavior in fragile X syndrome | 3 | 5 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1041 | 3 | 6 | 1764 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 87(5):436-439 Einfeld S; Tonge B; Turner G Longitudinal course of behavioral and emotional problems in Fragile X syndrome | 5 | 5 |
| 1042 | 59 | 96 | 1796 1999 INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE 3(6):639-645 Pimentel MMG Fragile X syndrome | 0 | 5 |
| 1043 | 18 | 28 | 1811 1999 JOURNAL OF MEDICAL SCREENING 6(2):70-76 Wildhagen MF; van Os TAM; Polder JJ; ten Kate LP; Habbema JDF Efficacy of cascade testing for fragile X syndrome | 3 | 5 |
| 1044 | 1 | 1 | 1819 1999 NATURE GENETICS 22(2):209-209 Coffee B Acetylated histones are associated with FMR1 in normal but not fragile X-syndrome cells (vol 22, pg 98, 1999) | 2 | 5 |
| 1045 | 3 | 3 | 1830 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(1):256-258 Hundscheid RDL; Thomas CMG; Braat DDM; Oostra BA; Smits APT Premature ovarian failure is associated with maternally and paternally inherited premutation in Brazilian families with fragile X - Reply | 2 | 5 |
| 1046 | 20 | 33 | 1881 2000 CLINICAL GENETICS 58(2):111-115 Kallinen J; Heinonen S; Mannermaa A; Ryynanen M Prenatal diagnosis of fragile X syndrome and the risk of expansion of a premutation | 3 | 5 |
| 1047 | 36 | 66 | 1936 2000 JOURNAL OF MEDICAL GENETICS 37(11):842-850 Salat U; Bardoni B; Wohrle D; Steinbach P Increase of FMRP expression, raised levels of FMR1 mRNA, and clonal selection in proliferating cells with unmethylated fragile X repeat expansions: a clue to the sex bias in the transmission of full mutations? | 2 | 5 |
| 1048 | 22 | 29 | 1944 2000 MENTAL RETARDATION 38(3):207-215 Maes B; Fryns JP; Ghesquiere P; Borghgraef M Phenotypic checklist to screen for fragile X syndrome in people with mental retardation | 2 | 5 |
| 1049 | 27 | 39 | 1988 2001 AMERICAN JOURNAL OF MEDICAL GENETICS 103(4):314-319 Johnston C; Eliez S; Dyer-Friedman J; Hessl D; Glaser B; Blasey C; Taylor A; Reiss A Neurobehavioral phenotype in carriers of the fragile X premutation | 5 | 5 |
| 1050 | 16 | 58 | 1995 2001 AMERICAN JOURNAL ON MENTAL RETARDATION 106(5):389-400 Sudhalter V; Belser RC Conversational characteristics of children with fragile x syndrome: Tangential language | 3 | 5 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1051 | 13 | 27 | 2075 2001 SEIZURE-EUROPEAN JOURNAL OF EPILEPSY 10(1):60-63 Sabaratnam M; Vroegop PG; Gangadharan SK Epilepsy and EEG findings in 18 males with fragile X syndrome | 4 | 5 |
| 1052 | 18 | 62 | 2096 2002 AMERICAN JOURNAL OF MEDICAL GENETICS 108(2):105-116 Hatton DD; Hooper SR; Bailey DB; Skinner ML; Sullivan KM; Wheeler A Problem behavior in boys with fragile X syndrome | 4 | 5 |
| 1053 | 32 | 51 | 2152 2002 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 23(6):416-423 Loesch DZ; Huggins RM; Bui QM; Epstein JL; Taylor AK; Hagerman RJ Effect of the deficits of fragile X mental retardation protein on cognitive status of fragile X males and females assessed by robust pedigree analysis | 5 | 5 |
| 1054 | 13 | 25 | 2158 2002 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 41(3):237-244 Dyer-Friedman J; Glaser B; Hessl D; Johnston C; Huffman LC; Taylor A; Wisbeck J; Reiss AL Genetic and environmental influences on the cognitive outcomes of children with fragile X syndrome | 5 | 5 |
| 1055 | 20 | 42 | 2166 2002 MICROSCOPY RESEARCH AND TECHNIQUE 57(3):159-167 Kates WR; Folley BS; Lanham DC; Capone GT; Kaufmann WE Cerebral growth in fragile X syndrome: Review and comparison with Down syndrome | 2 | 5 |
| 1056 | 33 | 52 | 2169 2002 MICROSCOPY RESEARCH AND TECHNIQUE 57(3):179-186 Keysor CS; Mazzocco MMM A developmental approach to understanding fragile X syndrome in females | 5 | 5 |
| 1057 | 0 | 3 | 44 1982 AMERICAN JOURNAL OF HUMAN GENETICS 34(6):A130-A130 JENKINS E; BROWN T; DUNCAN C; BROOKS J FRAGILE X-CHROMOSOME PRENATAL-DIAGNOSIS | 3 | 4 |
| 1058 | 0 | 0 | 90 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A92-A92 HAGERMAN R; MCBOGG P; LEVITUS A; MCGAVRAN L; SMITH A; BERRY B; BRADEN M; VANHOUSEN K; NEWALL K; MATUS I FOLIC-ACID TREATMENT OF THE FRAGILE-X SYNDROME | 3 | 4 |
| 1059 | 0 | 0 | 96 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A136-A136 JENKINS E; DUNCAN C; BROOKS J; LELE K; SANZ M; NOLIN S; BROWN T LOW-FREQUENCY FRAGILE X-CHROMOSOMES IN CULTURES FROM NORMAL PEOPLE | 0 | 4 |
| 1060 | 4 | 5 | 106 1983 AMERICAN JOURNAL OF MEDICAL GENETICS 14(4):795-796 DAKER MG FRAGILE X-CHROMOSOME IN NORMAL MALES | 2 | 4 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1061 | 2 | 15 | 112 1983 ANNALES DE GENETIQUE 26(3):171-173 JACKY PB; DILL FJ FRAGILE-X CHROMOSOME AND CHROMOSOME CONDENSATION | 1 | 4 |
| 1062 | 3 | 9 | 137 1983 HUMAN GENETICS 65(1):88-89 SOUDEK D; EMANUEL M A FRAGILE X SUPPRESSOR IN THE NORMAL HUMAN-BLOOD | 3 | 4 |
| 1063 | 3 | 8 | 159 1983 PRENATAL DIAGNOSIS 3(4):367-369 NIELSEN LB; NIELSEN KB; TOMMERUP N FRAGILE-X DEMONSTRATED RETROSPECTIVELY IN AMNIOTIC CELLS CULTURED IN LOW FOLATE MEDIUM | 2 | 4 |
| 1064 | 0 | 0 | 200 1984 EUROPEAN JOURNAL OF PEDIATRICS 141(4):265-265 LARGO RH; SCHINZEL A DEVELOPMENTAL AND BEHAVIORAL DISTURBANCES IN BOYS WITH THE FRAGILE-X SYNDROME | 1 | 4 |
| 1065 | 1 | 3 | 214 1984 JOURNAL OF MEDICAL GENETICS 21(1):74-75 SUTHERLAND GR ROUTINE DIAGNOSTIC-DETECTION OF THE FRAGILE X | 1 | 4 |
| 1066 | 1 | 4 | 221 1984 LANCET 1(8370):220-220 WEBB T; THAKE A; TODD J; BUNDEY S PREVALENCE OF FRAGILE X-CHROMOSOME | 2 | 4 |
| 1067 | 0 | 4 | 223 1984 LANCET 1(8370):220-221 LINNA SL; SIMILA S; HARO E; HERVA R PREVALENCE OF FRAGILE X-CHROMOSOME | 2 | 4 |
| 1068 | 3 | 6 | 232 1984 PRENATAL DIAGNOSIS 4(6):473-474 VENTER PA; COETZEE DJ; BADENHORST A; MARX MP; HOF JO; BEHARI D; WILMOT J; BATTSON SA A CONFIRMED PRENATAL-DIAGNOSIS OF A FEMALE FETUS WITH THE FRAGILE X-CHROMOSOME | 1 | 4 |
| 1069 | 0 | 3 | 257 1985 CANADIAN MEDICAL ASSOCIATION JOURNAL 133(5):358-& SOUDEK D FRAGILE-X - A SYMPTOM OF THE DISEASE | 2 | 4 |
| 1070 | 0 | 0 | 262 1985 CLINICAL GENETICS 27(3):334-335 SCHMIDT A PRENATAL-DIAGNOSIS OF FRAGILE X-SYNDROME | 2 | 4 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1071 | 0 | 4 | 275 1985 CYTOGENETICS AND CELL GENETICS 40(1-4):726-726 PURRELLO M; ALHADEFF B; ROCCHI M; ARCHIDIACONO N; DRAYNA D; SINISCALCO M RELATIVE POSITIVE OF POLYMORPHIC DNA LOCI OF THE HUMAN X-CHROMOSOME LONG ARM SUBTELOMERIC REGION WITH RESPECT TO THE FRAGILE X SITE (FRAXQ27) | 1 | 4 |
| 1072 | 5 | 11 | 342 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):511-514 HOWARDPEEBLES PN METHIONINE METABOLISM AND FRAGILE-X EXPRESSION | 0 | 4 |
| 1073 | 4 | 4 | 343 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):527-530 TOMMERUP N; HOLMGREN G; STEINBACH P FRAGILE-X - CARRIER DETECTION IN PREGNANCY | 1 | 4 |
| 1074 | 0 | 0 | 360 1986 ANNALS OF NEUROLOGY 20(3):417-417 PAYTON JB; STEELE MW; WENGER SL; MINSHEW NJ ASSOCIATION OF THE FRAGILE-X CHROMOSOME ABNORMALITY WITH INFANTILE-AUTISM | 4 | 4 |
| 1075 | 6 | 10 | 418 1987 AMERICAN JOURNAL OF MEDICAL GENETICS 27(3):731-732 CARPENTER NJ; VEENEMA H; BAKKER E; HOFKER MH; PEARSON PL A NEW DNA PROBE PROXIMAL TO AND CLOSELY LINKED TO FRAGILE-X | 4 | 4 |
| 1076 | 2 | 4 | 522 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):227-230 HOWARDPEEBLES PN; BROWN WT THE FRAGILE-X SYNDROME - VARIABILITY OF EXPRESSION IN CARRIER FEMALES | 3 | 4 |
| 1077 | 14 | 27 | 538 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):531-542 SCHWARTZ CE; PHELAN MC; BRIGHTHARP C; PANCOAST I; HOWARDPEEBLES PN; THIBODEAU S; BROWN WT; JENKINS EC FRAGILE-X SYNDROME - LINKAGE ANALYSIS IN BLACK AND WHITE-POPULATIONS | 4 | 4 |
| 1078 | 7 | 21 | 574 1988 CLINICAL GENETICS 34(4):265-271 ANVRET M; GILLBERG C; WAHLSTROM J; ALBERTSSONWIKLAND K; DAVIES K INFANTILE-AUTISM, FRAGILE (X) (Q27.3) AND RFLP ANALYSIS IN AN EXTENDED SWEDISH FAMILY | 2 | 4 |
| 1079 | 6 | 24 | 577 1988 CYTOGENETICS AND CELL GENETICS 48(3):142-147 FANTES J; GOSDEN J; PIPER J USE OF AN ALPHOID SATELLITE SEQUENCE TO LOCATE THE X-CHROMOSOME AUTOMATICALLY, WITH PARTICULAR REFERENCE TO IDENTIFICATION OF THE FRAGILE-X | 0 | 4 |
| 1080 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1081 | 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 |
| 1082 | 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 |
| 1083 | 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 |
| 1084 | 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 |
| 1085 | 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 |
| 1086 | 12 | 23 | 788 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):292-297 BROWN WT; GROSS A; GOONEWARDENA P; FERRANDO C; DOBKIN C; JENKINS EC DETECTION OF FRAGILE-X NON-PENETRANT MALES BY DNA MARKER ANALYSIS | 4 | 4 |
| 1087 | 2 | 4 | 814 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):445-446 HOWARDPEEBLES PN FRAGILE-X EXPRESSION - USE OF A DOUBLE INDUCTION SYSTEM | 2 | 4 |
| 1088 | 9 | 28 | 846 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 |
| 1089 | 4 | 15 | 866 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 | 1 | 4 |
| 1090 | 11 | 23 | 893 1991 PRENATAL DIAGNOSIS 11(5):333-338 WEBB T EXPRESSION OF FRAGILE-X IN A FEMALE FETUS DIAGNOSED AFTER CHORIONIC VILLUS SAMPLING | 3 | 4 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1091 | 0 | 0 | 896 1991 SCIENCE 252(5009):1070-1070 HOFFMAN M UNRAVELING THE GENETICS OF FRAGILE X-SYNDROME | 2 | 4 |
| 1092 | 5 | 11 | 916 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):96-102 BROWN WT; JENKINS EC; GOONEWARDENA P; MIEZEJESKI C; ATKIN J; DEVYS D PRENATALLY DETECTED FRAGILE-X FEMALES - LONG-TERM FOLLOW-UP-STUDIES SHOW HIGH-RISK OF MENTAL IMPAIRMENT | 4 | 4 |
| 1093 | 14 | 40 | 939 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):291-298 MIGEON BR CONCERNING THE ROLE OF X-INACTIVATION AND DNA METHYLATION IN FRAGILE X-SYNDROME | 3 | 4 |
| 1094 | 15 | 21 | 943 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):320-327 VANOOST BA; SMITS APT; DREESEN JCFM; VANDENOUWELAND AMW; OOSTRA BA VALIDATION OF LINKAGE-BASED DNA-DIAGNOSIS OF FRAGILE-X GENE CARRIERS WITH THE CGG REPEAT PROBE | 2 | 4 |
| 1095 | 6 | 8 | 948 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):355-360 SHERMAN SL; BARBI G; BRONDUMNIELSEN K; BROWN WT; CARPENTER NJ; CHUDLEY AE; FERRAZ OP; FERREIRA P; GUSTAVSON KH; HALLIDAY J; HOCKEY A; HOWARDPEEBLES PN; JENKINS E; KENNERKNECHT I; KAHKONEN M; LADAIQUE P; LEISTI J; MADDALENA A; MAZURCZAK T; MATTEI JF; MATTINA T; MCKINLEY MJ; MURPHY P; PELLISSIER MC; PURVISSMITH S; ROBINSON H; SCAPAGNINI U; SCHAAP T; SHAPIRO LR; SMITS APT; STEINBACH P; TURNER G; UCHIDA IA; VANOOST BA; VOELCKEL MA; WEAVER DD; WEBB T COLLABORATIVE PROSPECTIVE-STUDY OF THE FRAGILE-X SYNDROME - ONE-YEAR PROGRESS REPORT | 2 | 4 |
| 1096 | 2 | 2 | 990 1992 JOURNAL OF MEDICAL GENETICS 29(4):287-287 SMART RD FRAGILE X-SYNDROME - AS COMMON AS 1ST THOUGHT | 2 | 4 |
| 1097 | 3 | 10 | 992 1992 JOURNAL OF MEDICAL GENETICS 29(8):599-599 TIZZANO EF; BAIGET M HIGH PROPORTION OF TWINS IN CARRIERS OF FRAGILE X-SYNDROME | 3 | 4 |
| 1098 | 8 | 14 | 1021 1993 AMERICAN JOURNAL OF DISEASES OF CHILDREN 147(6):605-606 GOLDSON E; HAGERMAN RJ FRAGILE-X SYNDROME AND FAILURE-TO-THRIVE | 4 | 4 |
| 1099 | 13 | 25 | 1060 1993 AMERICAN JOURNAL OF MEDICAL GENETICS 45(5):589-593 MILUNSKY A; HUANG XL; AMOS JA; HERSKOWITZ J; FARRER LA; WYANDT HE 46,XY/47,XYY MALE WITH THE FRAGILE X-SYNDROME - CYTOGENETIC AND MOLECULAR STUDIES | 3 | 4 |
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