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Nodes: 2647,
Authors: 5321,
Journals: 428,
Outer References: 16458,
Words: 3536
Collection span: 1967 - 2005
View: Overview. Sorted by GCS.
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| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 901 | 3 | 9 | 186 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):299-301 ERBE RW FOLIC-ACID THERAPY IN THE FRAGILE-X SYNDROME | 4 | 8 |
| 902 | 9 | 44 | 281 1985 DISEASE MARKERS 3(1):9-25 JACOBS PA; SHERMAN SL THE FRAGILE(X) - A MARKER FOR THE MARTIN-BELL SYNDROME | 6 | 8 |
| 903 | 14 | 32 | 283 1985 HELVETICA PAEDIATRICA ACTA 40(2-3):133-152 SCHINZEL A; LARGO RH THE FRAGILE X-SYNDROME (MARTIN-BELL SYNDROME) - CLINICAL AND CYTOGENETIC FINDINGS IN 16 PREPUBERTAL BOYS AND IN 4 OF THEIR 5 FAMILIES | 4 | 8 |
| 904 | 2 | 8 | 324 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):179-187 SHELLHART WC; CASAMASSIMO PS; HAGERMAN RJ; BELANGER GK ORAL FINDINGS IN FRAGILE-X SYNDROME | 4 | 8 |
| 905 | 8 | 16 | 343 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 |
| 906 | 18 | 55 | 357 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):723-737 VANDYKE DL; WEISS L MATERNAL EFFECT ON INTELLIGENCE IN FRAGILE-X MALES AND FEMALES | 4 | 8 |
| 907 | 9 | 16 | 398 1986 JOURNAL OF MEDICAL GENETICS 23(5):400-406 WEBB T; THAKE A; TODD J 12 FAMILIES WITH FRAGILE X(Q27) | 7 | 8 |
| 908 | 4 | 18 | 480 1987 JOURNAL OF MENTAL DEFICIENCY RESEARCH 31:73-79 PUESCHEL SM; OBRIEN MM; PADREMENDOZA T KLINEFELTER SYNDROME AND ASSOCIATED FRAGILE-X SYNDROME | 7 | 8 |
| 909 | 5 | 22 | 518 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):115-121 WATSON MS; BREG WR; PAULS D; BROWN WT; CARROLL AJ; et al. ANEUPLOIDY AND THE FRAGILE-X SYNDROME | 6 | 8 |
| 910 | 3 | 3 | 536 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 911 | 3 | 4 | 547 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 |
| 912 | 2 | 15 | 560 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 31(4):767-773 BUTLER MG; FLETCHER M; GALE DD; MEANEY FJ; MCLEOD DR; et al. METACARPOPHALANGEAL PATTERN PROFILE ANALYSIS IN FRAGILE-X SYNDROME | 4 | 8 |
| 913 | 16 | 34 | 587 1988 HUMAN GENETICS 78(4):338-342 CLAYTON JF; GOSDEN CM; HASTIE ND; EVANS HJ LINKAGE HETEROGENEITY AND FRAGILE-X | 4 | 8 |
| 914 | 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 |
| 915 | 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 |
| 916 | 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 |
| 917 | 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 |
| 918 | 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 |
| 919 | 4 | 4 | 874 1991 JOURNAL OF MEDICAL GENETICS 28(5):358-358 WEBB T; BUNDEY S PREVALENCE OF FRAGILE X-SYNDROME | 6 | 8 |
| 920 | 5 | 29 | 910 1992 AMERICAN JOURNAL OF HUMAN GENETICS 50(5):1067-1076 LOESCH DZ; HUGGINS RM FIXED AND RANDOM EFFECTS IN THE VARIATION OF THE FINGER RIDGE COUNT - A STUDY OF FRAGILE-X FAMILIES | 7 | 8 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 921 | 24 | 31 | 914 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):5-27 MANDEL JL; HAGERMAN R; FROSTER U; BROWN WT; JENKINS EC; et al. 5TH INTERNATIONAL WORKSHOP ON THE FRAGILE-X AND X-LINKED MENTAL-RETARDATION | 5 | 8 |
| 922 | 15 | 23 | 923 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):87-95 HINTON VJ; DOBKIN CS; HALPERIN JM; JENKINS EC; BROWN WT; et al. MODE OF INHERITANCE INFLUENCES BEHAVIORAL EXPRESSION AND MOLECULAR CONTROL OF COGNITIVE DEFICITS IN FEMALE CARRIERS OF THE FRAGILE-X SYNDROME | 5 | 8 |
| 923 | 11 | 29 | 925 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):111-115 GRIGSBY J; KEMPER MB; HAGERMAN RJ VERBAL-LEARNING AND MEMORY AMONG HETEROZYGOUS FRAGILE-X FEMALES | 8 | 8 |
| 924 | 9 | 13 | 945 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):261-267 SMITS A; SMEETS D; DREESEN J; HAMEL B; DEHAAN A; et al. PARENTAL ORIGIN OF THE FRA(X) GENE IS A MAJOR DETERMINANT OF THE CYTOGENETIC EXPRESSION AND THE CGG REPEAT LENGTH IN FEMALE CARRIERS | 4 | 8 |
| 925 | 4 | 6 | 953 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):328-332 NOLIN SL; SNIDER DA; JENKINS EC; DOBKIN CS; PATCHELL K; et al. NEW-YORK-STATE SCREENING-PROGRAM FOR FRAGILE-X SYNDROME - A PROGRESS REPORT | 7 | 8 |
| 926 | 6 | 24 | 987 1992 GENOMICS 12(4):814-817 FAUST CJ; VERKERK AJMH; WILSON PJ; MORRIS CP; HOPWOOD JJ; et al. GENETIC-MAPPING ON THE MOUSE X-CHROMOSOME OF HUMAN CDNA CLONES FOR THE FRAGILE-X AND HUNTER SYNDROMES | 0 | 8 |
| 927 | 11 | 16 | 1015 1992 NATURE GENETICS 1(3):157-158 HAGERMAN R CLINICAL CONUNDRUMS IN FRAGILE-X SYNDROME | 7 | 8 |
| 928 | 7 | 7 | 1093 1993 CLINICAL GENETICS 43(3):157-159 MORNET E; JOKIC M; BOGYO A; TEJADA I; DELUCHAT C; et al. AFFECTED SIBS WITH FRAGILE-X SYNDROME EXHIBIT AN AGE-DEPENDENT DECREASE IN THE SIZE OF THE FRAGILE-X FULL MUTATION | 8 | 8 |
| 929 | 18 | 37 | 1096 1993 CLINICAL GENETICS 44(3):129-138 BUTLER MG; PRATESI R; WATSON MS; BREG WR; SINGH DN ANTHROPOMETRIC AND CRANIOFACIAL PATTERNS IN MENTALLY-RETARDED MALES WITH EMPHASIS ON THE FRAGILE-X SYNDROME | 4 | 8 |
| 930 | 17 | 34 | 1098 1993 CURRENT BIOLOGY 3(11):783-786 TROTTIER Y; DEVYS D; MANDEL JL FRAGILE-X SYNDROME - AN EXPANDING STORY | 4 | 8 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 931 | 23 | 40 | 1124 1993 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 23(1):201-209 HASHIMOTO O; SHIMIZU Y; KAWASAKI Y LOW-FREQUENCY OF THE FRAGILE-X SYNDROME AMONG JAPANESE AUTISTIC SUBJECTS | 3 | 8 |
| 932 | 3 | 4 | 1142 1993 LANCET 341(8847):770-770 BUNDEY S; NORMAN E POPULATION SCREENING FOR FRAGILE-X SYNDROME | 8 | 8 |
| 933 | 4 | 7 | 1184 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):370-373 STEYAERT J; DECRUYENAERE M; BORGHGRAEF M; FRYNS JP PERSONALITY PROFILE IN ADULT FEMALE FRAGILE-X CARRIERS - ASSESSED WITH THE MINNESOTA MULTIPHASIC PERSONALITY PROFILE (MMPI) | 3 | 8 |
| 934 | 4 | 15 | 1195 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):447-450 POMPONI MG; NERI G BUTYRATE AND ACETYL-CARNITINE INHIBIT THE CYTOGENETIC EXPRESSION OF THE FRAGILE-X IN-VITRO | 2 | 8 |
| 935 | 15 | 19 | 1199 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):458-462 TURNER AM; ROBINSON H; WAKE S; LAING SJ; LEIGH D; et al. 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 |
| 936 | 8 | 10 | 1205 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):486-489 VONKOSKULL H; GAHMBERG N; SALONEN R; SALO A; PEIPPO M FRAXA LOCUS IN FRAGILE-X DIAGNOSIS - FAMILY STUDIES, PRENATAL-DIAGNOSIS, AND DIAGNOSIS OF SPORADIC CASES OF MENTAL-RETARDATION | 8 | 8 |
| 937 | 0 | 19 | 1234 1994 GENES CHROMOSOMES & CANCER 9(2):141-144 RIGGINS GJ; SHERMAN SL; PHILLIPS CN; STOCK W; WESTBROOK CA; et al. CGG-REPEAT POLYMORPHISM OF THE BCR GENE RULES OUT PREDISPOSING ALLELES LEADING TO THE PHILADELPHIA-CHROMOSOME | 1 | 8 |
| 938 | 1 | 5 | 1248 1994 ITALIAN JOURNAL OF NEUROLOGICAL SCIENCES 15(7):365-368 MUSUMECI SA; ELIA M; FERRI R; SCUDERI C; DELGRACCO S EVOKED SPIKES AND GIANT SOMATOSENSORY-EVOKED POTENTIALS IN A PATIENT WITH FRAGILE-X SYNDROME | 3 | 8 |
| 939 | 16 | 27 | 1257 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 |
| 940 | 3 | 8 | 1258 1994 JOURNAL OF MEDICAL GENETICS 31(1):76-78 TEJADA MI; MORNET E; TIZZANO E; MOLINA M; BAIGET M; et al. IDENTIFICATION BY MOLECULAR DIAGNOSIS OF MOSAIC TURNERS-SYNDROME IN AN OBLIGATE CARRIER FEMALE FOR FRAGILE-X SYNDROME | 4 | 8 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 941 | 14 | 21 | 1328 1995 AMERICAN JOURNAL OF MEDICAL GENETICS 59(4):426-430 MCCONKIEROSELL A; ROBINSON H; WAKE S; STALEY LW; HELLER K; et al. DISSEMINATION OF GENETIC RISK INFORMATION TO RELATIVES IN THE FRAGILE-X SYNDROME - GUIDELINES FOR GENETIC COUNSELORS | 7 | 8 |
| 942 | 12 | 24 | 1333 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 |
| 943 | 12 | 31 | 1482 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 | 6 | 8 |
| 944 | 40 | 74 | 1523 1996 COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY 61:679-687 Eberhart DE; Warren ST The molecular basis of fragile X syndrome | 7 | 8 |
| 945 | 60 | 94 | 1526 1996 DEVELOPMENTAL PSYCHOLOGY 32(3):416-424 Hagerman RJ Biomedical advances in developmental psychology: The case of fragile X syndrome | 3 | 8 |
| 946 | 19 | 26 | 1535 1996 HUMAN GENETICS 97(4):512-515 Mornet E; Chateau C; Taillandier A; SimonBouy B; Serre JL Recurrent and unexpected segregation of the FMR1 CGG repeat in a family with fragile X syndrome | 6 | 8 |
| 947 | 14 | 17 | 1570 1996 PEDIATRICS 98(2):297-300 Desposito F; Cho S; Frias JL; Sherman J; Wappner RS; et al. Health supervision for children with fragile X syndrome | 3 | 8 |
| 948 | 22 | 32 | 1630 1997 ANNALES DE GENETIQUE 40(3):139-144 Gerard B; LeHeuzey MF; Brunie G; Lewine P; Saiag MC; et al. Systematic screening for fragile X syndrome in a cohort of 574 mentally retarded children | 4 | 8 |
| 949 | 28 | 43 | 1634 1997 ANNALS OF MEDICINE 29(6):563-567 Oostra BA; Hoogeveen AT Animal model for fragile X syndrome | 3 | 8 |
| 950 | 4 | 22 | 1665 1997 HUMAN HEREDITY 47(5):254-262 Gurling HMD; Bolton PF; Vincent J; Melmer G; Rutter M Molecular and cytogenetic investigations of the fragile X region including the Frax A and Frax E CGG trinucleotide repeat sequences in families multiplex for autism and related phenotypes | 0 | 8 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 951 | 76 | 123 | 1710 1997 WESTERN JOURNAL OF MEDICINE 166(2):129-137 Hagerman RJ Fragile X syndrome - Molecular and clinical insights and treatment issues | 6 | 8 |
| 952 | 23 | 41 | 1748 1998 HUMAN GENETICS 102(4):440-445 Gronskov K; Hallberg A; Brondum-Nielsen K Mutational analysis of the FMR1 gene in 118 mentally retarded males suspected of fragile X syndrome: absence of prevalent mutations | 4 | 8 |
| 953 | 24 | 41 | 1773 1998 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 42:81-89 Elbaz A; Suedois J; Duquesnoy M; Beldjord C; Berchel C; et al. Prevalence of fragile-X syndrome and FRAXE among children with intellectual disability in a Caribbean island, Guadeloupe, French West Indies | 6 | 8 |
| 954 | 0 | 5 | 1823 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(2):140-141 Hjalgrim H; Jacobsen TB; Norgaard K; Lou HC; Brondum-Nielsen K; et al. Frontal-subcortical hypofunction in the fragile X syndrome | 5 | 8 |
| 955 | 8 | 23 | 1826 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):253-256 Fisch GS; Holden JJK; Carpenter NJ; Howard-Peebles PN; Maddalena A; et al. Age-related language characteristics of children and adolescents with fragile X syndrome | 7 | 8 |
| 956 | 10 | 20 | 1854 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):226-228 Glaser D; Wohrle D; Salat U; Vogel W; Steinbach P; et al. Mitotic behavior of expanded CGG repeats studied on cultured cells: Further evidence for methylation-mediated triplet repeat stability in fragile X syndrome | 5 | 8 |
| 957 | 8 | 8 | 1938 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(1):11-13 Sherman SL Premature ovarian failure among fragile X premutation carriers: Parent-of-origin effect? | 4 | 8 |
| 958 | 12 | 16 | 2063 2000 JOURNAL OF MEDICAL GENETICS 37(8):603-604 Willemsen R; Olmer R; Otero YD; Oostra BA Twin sisters, monozygotic with the fragile X mutation, but with a different phenotype | 8 | 8 |
| 959 | 16 | 58 | 2124 2001 AMERICAN JOURNAL ON MENTAL RETARDATION 106(5):389-400 Sudhalter V; Belser RC Conversational characteristics of children with fragile x syndrome: Tangential language | 5 | 8 |
| 960 | 0 | 14 | 2167 2001 JOURNAL OF CRYSTAL GROWTH 226(1):101-106 Jung IH; Yoshikawa A; Lebbou K; Fukuda T; Auh KH Crystal growth by micro-pulling-down of Ca3Ga2Ge4O14 (CGG) type-Sr3Nb1-xGa3 (+) (5/3)xSi2O14 compounds | 0 | 8 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 961 | 11 | 91 | 2173 2001 JOURNAL OF LEARNING DISABILITIES 34(6):520-533 Mazzocco MMM Math learning disability and math LD subtypes: Evidence from studies of Turner syndrome, fragile X syndrome, and neurofibromatosis type 1 | 2 | 8 |
| 962 | 25 | 40 | 2192 2001 PEDIATRICS 108(5):art. no.-e88 Hessl D; Dyer-Friedman J; Glaser B; Wisbeck J; Barajas RG; et al. The influence of environmental and genetic factors on behavior problems and autistic symptoms in boys and girls with fragile X syndrome | 0 | 8 |
| 963 | 42 | 139 | 2262 2002 DEVELOPMENTAL PSYCHOBIOLOGY 40(3):323-338 Churchill JD; Grossman AW; Irwin SA; Galvez R; Klintsova AY; et al. A converging-methods approach to fragile X syndrome | 2 | 8 |
| 964 | 9 | 20 | 2331 2002 NEURON 34(6):859-862 Gao FB Understanding fragile X syndrome: Insights from retarded flies | 6 | 8 |
| 965 | 15 | 32 | 2333 2002 NEUROPSYCHOLOGIA 40(8):1343-1349 Wilding J; Cornish K; Munir F Further delineation of the executive deficit in males with fragile-X syndrome | 7 | 8 |
| 966 | 13 | 15 | 2347 2002 TRENDS IN MOLECULAR MEDICINE 8(3):102-103 Oostra BA Functions of the fragile X protein | 6 | 8 |
| 967 | 20 | 46 | 2383 2003 AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS 121B(1):119-127 Aziz M; Stathopulu E; Callias M; Taylor C; Turk J; et al. Clinical features of boys with fragile X premutations and intermediate alleles | 0 | 8 |
| 968 | 38 | 53 | 2403 2003 BIOLOGY OF THE CELL 95(3-4):221-228 Schaeffer C; Beaulande M; Ehresmann C; Ehresmann B; Moine H The RNA binding protein FMRP: new connections and missing links | 3 | 8 |
| 969 | 39 | 53 | 2429 2003 HUMAN MOLECULAR GENETICS 12(14):1689-1698 Bardoni B; Castets M; Huot ME; Schenck A; Adinolfi S; et al. 82-FIP, a novel FMRP (Fragile X Mental Retardation Protein) interacting protein, shows a cell cycle-dependent intracellular localization | 8 | 8 |
| 970 | 2 | 4 | 19 1981 CLINICAL GENETICS 20(1):78-78 HOWARDPEEBLES PN FRAGILE-X CHROMOSOME IN NORMAL MALES | 4 | 7 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 971 | 0 | 0 | 44 1982 AMERICAN JOURNAL OF HUMAN GENETICS 34(6):A110-A110 SHAPIRO LR; HASEN J; GORDON G; SOUTHREN AL; WILMOT PL; et al. TESTICULAR INSUFFICIENCY AND DISORDERED THYROID METABOLISM IN THE FRAGILE X-CHROMOSOME SYNDROME | 5 | 7 |
| 972 | 0 | 1 | 151 1983 JOURNAL OF MEDICAL GENETICS 20(6):476-476 MORICPETROVIC S; LACA Z A FATHER AND DAUGHTER WITH FRAGILE X-CHROMOSOME | 6 | 7 |
| 973 | 8 | 12 | 188 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(4):853-855 GARDNER RJM FRAGILE-X MALES WITH NORMAL INTELLIGENCE - AND IF SO, WHY | 4 | 7 |
| 974 | 1 | 9 | 195 1984 CLINICAL GENETICS 25(2):135-139 GARDINER GB; WENGER SL; STEELE MW INVITRO REVERSAL OF FRAGILE-X EXPRESSION BY EXOGENOUS THYMIDINE | 5 | 7 |
| 975 | 3 | 24 | 206 1984 HUMAN GENETICS 67(1):99-102 CANTU ES; JACOBS PA FRAGILE (X) EXPRESSION - RELATIONSHIP TO THE CELL-CYCLE | 4 | 7 |
| 976 | 8 | 18 | 321 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):111-126 PARTINGTON MW FEMALE RELATIVES IN FAMILIES WITH THE FRAGILE X-SYNDROME | 4 | 7 |
| 977 | 13 | 30 | 428 1987 ARCHIVES OF OPHTHALMOLOGY 105(8):1099-1102 STORM RL; PEBENITO R; FERRETTI C OPHTHALMOLOGIC FINDINGS IN THE FRAGILE X-SYNDROME | 5 | 7 |
| 978 | 0 | 0 | 444 1987 CYTOGENETICS AND CELL GENETICS 46(1-4):587-587 BROWN WT; WU Y; GROSS AC; CHAN CB; DOBKIN CS; et al. LINKAGE OF FLANKING PROBES IN 40 FRAGILE X-FAMILIES | 1 | 7 |
| 979 | 4 | 5 | 548 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 |
| 980 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 981 | 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 |
| 982 | 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 |
| 983 | 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 |
| 984 | 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 |
| 985 | 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 |
| 986 | 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 |
| 987 | 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 |
| 988 | 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 |
| 989 | 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 |
| 990 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 991 | 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 |
| 992 | 7 | 11 | 891 1991 NATURE 351(6326):439-440 DAVIES K HUMAN-GENETICS - BREAKING THE FRAGILE-X | 2 | 7 |
| 993 | 10 | 17 | 938 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 | 7 | 7 |
| 994 | 12 | 15 | 947 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):282-290 TEJADA I; MORNET E; BIANCALANA V; OBERLE I; BOUE J; et al. DIRECT DNA ANALYSIS OF FRAGILE-X SYNDROME IN SPANISH PEDIGREES | 7 | 7 |
| 995 | 3 | 3 | 956 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):353-354 DRUGGE U; HOLMGREN G; SONBLOMQUIST HK; DAHL N; GUSTAVSON KH; et al. STUDY OF INDIVIDUALS POSSIBLY AFFECTED WITH THE FRAGILE-X SYNDROME IN A LARGE SWEDISH FAMILY IN THE 18TH TO 20TH CENTURIES | 7 | 7 |
| 996 | 16 | 32 | 964 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 44(6):816-821 DEWALD GW; BUCKLEY DD; SPURBECK JL; JALAL SM CYTOGENETIC GUIDELINES FOR FRAGILE-X STUDIES TESTED IN ROUTINE PRACTICE | 3 | 7 |
| 997 | 6 | 10 | 995 1992 JAPANESE JOURNAL OF HUMAN GENETICS 37(3):195-203 YAMAUCHI M; SEKI N; HORI TA RAPID PREPARATION OF DIAGNOSTIC PROBES FOR THE FRAGILE-X SYNDROME BY DIRECT PCR AMPLIFICATION OF HUMAN CHROMOSOMAL DNA | 4 | 7 |
| 998 | 49 | 76 | 997 1992 JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY AND ALLIED DISCIPLINES 33(7):1127-1139 HAGERMAN RJ FRAGILE-X SYNDROME - ADVANCES AND CONTROVERSY | 3 | 7 |
| 999 | 27 | 59 | 1025 1992 PSYCHIATRIC GENETICS 2(4):277-300 BOLTON P; PICKLES A; BUTLER L; SUMMERS D; WEBB T; et al. FRAGILE-X IN FAMILIES MULTIPLEX FOR AUTISM AND RELATED PHENOTYPES - PREVALENCE AND CRITERIA FOR CYTOGENETIC DIAGNOSIS | 1 | 7 |
| 1000 | 1 | 1 | 1158 1993 NATURE GENETICS 5(3):312-312 HINDS HL; ASHLEY CT; SUTCLIFFE JS; NELSON DL; WARREN ST; et al. TISSUE-SPECIFIC EXPRESSION OF FMR-1 PROVIDES EVIDENCE FOR A FUNCTIONAL-ROLE IN FRAGILE X-SYNDROME (VOL 3, PG 36, 1993) | 6 | 7 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1001 | 6 | 13 | 1162 1993 PEDIATRICS 91(4):714-715 CRABBE LS; BENSKY AS; HORNSTEIN L; SCHWARTZ DC CARDIOVASCULAR-ABNORMALITIES IN CHILDREN WITH FRAGILE-X SYNDROME | 5 | 7 |
| 1002 | 26 | 42 | 1178 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):328-338 KOLEHMAINEN K; KARANT Y MODELING METHYLATION AND IQ SCORES IN FRAGILE-X FEMALES AND MOSAIC MALES | 4 | 7 |
| 1003 | 11 | 13 | 1325 1995 AMERICAN JOURNAL OF MEDICAL GENETICS 55(3):384-386 PRIOR TW; PAPP AC; SNYDER PJ; SEDRA MS; GUIDA M; et al. GERMLINE MOSAICISM AT THE FRAGILE-X LOCUS | 2 | 7 |
| 1004 | 9 | 28 | 1330 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 | 7 | 7 |
| 1005 | 0 | 24 | 1344 1995 BIOPHYSICAL JOURNAL 69(2):553-558 RAMAKRISHNAN B; SUNDARALINGAM M CRYSTAL-STRUCTURE OF THE A-DNA DECAMER D(CCIGGCCM(5)CGG) AT 1.6-ANGSTROM SHOWING THE UNEXPECTED WOBBLE I-CENTER-DOT-M(5)C BASE-PAIR | 0 | 7 |
| 1006 | 17 | 33 | 1393 1995 HUMAN GENETICS 96(3):323-329 DREESEN JCFM; GERAEDTS JPM; DUMOULIN JCM; EVERS JLH; PIETERS MHEC RS46(DXS548) GENOTYPING OF REPRODUCTIVE CELLS - APPROACHING PREIMPLANTATION TESTING OF THE FRAGILE-X SYNDROME | 2 | 7 |
| 1007 | 11 | 12 | 1457 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):176-180 Perroni L; Grasso M; Argusti A; LoNigro C; Croci GF; et al. Molecular and cytogenetic analysis of the fragile X syndrome in a series of 453 mentally retarded subjects: A study of 87 families | 6 | 7 |
| 1008 | 6 | 10 | 1633 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 | 6 | 7 |
| 1009 | 18 | 26 | 1644 1997 CLINICAL GENETICS 51(1):1-6 Loesch DZ; Petrovic V; Francis DI; Oertel R; Slater H ''Reduction'' of CGG trinucleotide expansion from mother to offspring in seven fragile-X families | 4 | 7 |
| 1010 | 11 | 15 | 1687 1997 JOURNAL OF MEDICAL GENETICS 34(11):924-926 Losekoot M; Hoogendoorn E; Olmer R; Jansen CCAM; Oosterwijk JC; et al. Prenatal diagnosis of the fragile X syndrome: loss of mutation owing to a double recombinant or gene conversion event at the FMR1 locus | 1 | 7 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1011 | 24 | 39 | 1713 1998 AMERICAN JOURNAL OF MEDICAL GENETICS 75(3):277-282 Jara L; Aspillaga M; Avendano I; Obreque V; Blanco R; et al. Distribution of (CGG)n and FMR-1 associated microsatellite alleles in a normal Chilean population | 6 | 7 |
| 1012 | 8 | 10 | 1727 1998 CLINICAL GENETICS 53(3):200-201 Mornet E; Chateau C; Simon-Bouy B; Serre JL The intermediate alleles of the fragile X CGG repeat in patients with mental retardation | 3 | 7 |
| 1013 | 0 | 28 | 1745 1998 GENOMICS 47(3):414-418 Albanese V; Holbert S; Saada C; Meier-Ewert S; Lebre AS; et al. CAG/CTG and CGG/GCC repeats in human brain reference cDNAs: Outcome in searching for new dynamic mutations | 0 | 7 |
| 1014 | 6 | 30 | 1765 1998 JOURNAL OF BIOLOGICAL CHEMISTRY 273(27):17122-17127 Bolivar J; Guelman S; Iglesias C; Ortiz M; Valdivia MM The fragile-X-related gene FXR1 is a human autoantigen processed during apoptosis | 3 | 7 |
| 1015 | 5 | 20 | 1822 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 82(3):206-211 McConkie-Rosell A; Spiridigliozzi GA; Rounds K; Dawson DV; Sullivan JA; et al. Parental attitudes regarding carrier testing in children at risk for fragile X syndrome | 2 | 7 |
| 1016 | 22 | 25 | 1853 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):221-225 Schmucker B; Seidel J Mosaicism for a full mutation and a normal size allele in two fragile X males | 5 | 7 |
| 1017 | 5 | 12 | 1867 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 87(4):366-368 Torrioli MG; Vernacotola S; Mariotti P; Bianchi E; Calvani M; et al. Double-blind, placebo-controlled study of L-acetylcarnitine for the treatment of hyperactive behavior in fragile X syndrome | 4 | 7 |
| 1018 | 0 | 18 | 2010 2000 EUROPEAN JOURNAL OF NEUROSCIENCE 12(1):381-384 Miller WJ; Skinner JA; Foss GS; Davies KE Localization of the fragile X mental retardation 2 (FMR2) protein in mammalian brain | 0 | 7 |
| 1019 | 27 | 59 | 2034 2000 JOURNAL OF BIOLOGICAL CHEMISTRY 275(42):33134-33141 Uliel L; Weisman-Shomer P; Oren-Jazans H; Newcomb T; Loeb LA; et al. Human Ku antigen tightly binds and stabilizes a tetrahelical form of the fragile X syndrome d(CGG)(n) expanded sequence | 1 | 7 |
| 1020 | 16 | 86 | 2144 2001 DEVELOPMENTAL PSYCHOBIOLOGY 39(2):107-123 Roberts JE; Boccia ML; Bailey DB; Hatton DD; Skinner M Cardiovascular indices of physiological arousal in boys with fragile X syndrome | 7 | 7 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1021 | 23 | 64 | 2159 2001 HUMAN MOLECULAR GENETICS 10(24):2803-2811 Huot ME; Mazroui R; Leclerc P; Khandjian EW Developmental expression of the fragile X-related 1 proteins in mouse testis: association with microtubule elements | 5 | 7 |
| 1022 | 9 | 18 | 2234 2002 AMERICAN JOURNAL OF MEDICAL GENETICS 107(2):136-142 Loesch DZ; Huggins RM; Taylor AK Application of robust pedigree analysis in studies of complex genotype-phenotype relationships in fragile X syndrome | 5 | 7 |
| 1023 | 18 | 62 | 2236 2002 AMERICAN JOURNAL OF MEDICAL GENETICS 108(2):105-116 Hatton DD; Hooper SR; Bailey DB; Skinner ML; Sullivan KM; et al. Problem behavior in boys with fragile X syndrome | 6 | 7 |
| 1024 | 9 | 26 | 2397 2003 BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 305(2):434-441 Dolzhanskaya N; Sung YJ; Conti J; Currie JR; Denman RB The fragile X mental retardation protein interacts with U-rich RNAs in a yeast three-hybrid system | 5 | 7 |
| 1025 | 27 | 40 | 2399 2003 BIOCHEMISTRY 42(35):10437-10444 Adinolfi S; Ramos A; Martin SR; Dal Piaz F; Pucci P; et al. The N-terminus of the fragile X mental retardation protein contains a novel domain involved in dimerization and RNA binding | 6 | 7 |
| 1026 | 19 | 33 | 2415 2003 CYTOGENETIC AND GENOME RESEARCH 100(1-4):206-212 Hagerman PJ; Greco CM; Hagerman RJ A cerebellar tremor/ataxia syndrome among fragile X premutation carriers | 4 | 7 |
| 1027 | 28 | 61 | 2420 2003 EXPERIMENTAL CELL RESEARCH 289(1):95-107 Bardoni B; Willemsen R; Weiler IJ; Schenck A; Severijnen LA; et al. NUFIP 1 (nuclear FMRP interacting protein 1) is a nucleocytoplasmic shuttling protein associated with active synaptoneurosome | 6 | 7 |
| 1028 | 10 | 23 | 2469 2003 NUCLEIC ACIDS RESEARCH 31(21):6243-6248 Handa V; Saha T; Usdin K The fragile X syndrome repeats form RNA hairpins that do not activate the interferon-inducible protein kinase, PKR, but are cut by Dicer | 3 | 7 |
| 1029 | 15 | 26 | 2481 2004 AMERICAN JOURNAL OF HUMAN GENETICS 74(5):1051-1056 Hagerman RJ; Leavitt BR; Farzin F; Jacquemont S; Greco CM; et al. Fragile-X-associated tremor/ataxia syndrome (FXTAS) in females with the FMR1 premutation | 3 | 7 |
| 1030 | 40 | 97 | 2560 2004 JOURNAL OF NEUROSCIENCE 24(25):5798-5809 Michel CI; Kraft R; Restifo LL Defective neuronal development in the mushroom bodies of Drosophila Fragile X Mental Retardation 1 Mutants | 6 | 7 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1031 | 26 | 61 | 2610 2004 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 101(36):13357-13362 Khandjian EW; Huot ME; Tremblay S; Davidovic L; Mazroui R; et al. Biochemical evidence for the association of fragile X mental retardation protein with brain polyribosomal ribonucleoparticles | 6 | 7 |
| 1032 | 2 | 6 | 157 1983 NEW ENGLAND JOURNAL OF MEDICINE 308(5):285-286 HECHT F; GLOVER TW ANTIBIOTICS CONTAINING TRIMETHOPRIM AND THE FRAGILE X-CHROMOSOME | 4 | 6 |
| 1033 | 0 | 2 | 181 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):253-254 DEV VG; MIXON C 5-AZACYTIDINE DECREASES THE FREQUENCY OF FRAGILE-X EXPRESSION IN PERIPHERAL LYMPHOCYTE CULTURE | 4 | 6 |
| 1034 | 3 | 23 | 233 1984 PEDIATRICS 74(5):883-886 CARMI R; MERYASH DL; WOOD J; GERALD PS FRAGILE-X SYNDROME ASCERTAINED BY THE PRESENCE OF MACRO-ORCHIDISM IN A 5-MONTH-OLD INFANT | 4 | 6 |
| 1035 | 3 | 19 | 257 1985 AMERICAN JOURNAL OF PUBLIC HEALTH 75(7):771-772 TRUSLER S; BEATTYDESANA J FRAGILE X-SYNDROME - A PUBLIC-HEALTH CONCERN | 5 | 6 |
| 1036 | 2 | 8 | 263 1985 CLINICAL GENETICS 27(2):118-121 HIRTH L; SINGH S; SCHILLING S; MULLER E; GOEDDE HW DERMATOGLYPHIC FINDINGS IN PATIENTS WITH FRAGILE X-CHROMOSOME | 2 | 6 |
| 1037 | 4 | 8 | 267 1985 CLINICAL GENETICS 27(5):520-521 WEBB GC DETECTION OF THE FRAGILE X-CHROMOSOME AND OTHER FRAGILE SITES | 5 | 6 |
| 1038 | 5 | 24 | 318 1986 AMERICAN JOURNAL OF HUMAN GENETICS 38(3):309-318 GLOVER TW; COYLEMORRIS J; PEARCEBIRGE L; BERGER C; GEMMILL RM DNA DEMETHYLATION INDUCED BY 5-AZACYTIDINE DOES NOT AFFECT FRAGILE-X EXPRESSION | 3 | 6 |
| 1039 | 4 | 11 | 327 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):207-211 WILLIAMS CA; CANTU ES; FRIAS JL BRIEF CLINICAL REPORT - METAPHYSEAL DYSOSTOSIS AND CONGENITAL NYSTAGMUS IN A MALE INFANT WITH THE FRAGILE-X SYNDROME | 2 | 6 |
| 1040 | 4 | 18 | 348 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):537-544 NIELSEN KB SEX-CHROMOSOME ANEUPLOIDY IN FRAGILE-X CARRIERS | 1 | 6 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1041 | 8 | 18 | 394 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 |
| 1042 | 12 | 26 | 413 1986 SOUTHERN MEDICAL JOURNAL 79(4):405-409 YOUNG RS; JARAMILLO C; MCCOMBS JL; MOORE CM; JORGENSON RJ FRAGILE-X MENTAL-RETARDATION SYNDROME TRANSMITTED THROUGH INTELLECTUALLY NORMAL MALES - IMPLICATIONS FOR GENETIC-COUNSELING | 3 | 6 |
| 1043 | 0 | 0 | 492 1987 PEDIATRIC NEUROLOGY 3(5):284-287 MATSUISHI T; SHIOTSUKI Y; NIIKAWA N; KATAFUCHI Y; OTAKI E; et al. FRAGILE-X SYNDROME IN JAPANESE PATIENTS WITH INFANTILE-AUTISM | 4 | 6 |
| 1044 | 1 | 2 | 528 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):237-238 EINFELD SL AUTISM AND THE FRAGILE-X SYNDROME | 4 | 6 |
| 1045 | 2 | 13 | 541 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):459-471 THODE A; LAING S; PARTINGTON MW; TURNER G IS THERE A FRAGILE(X) NEGATIVE MARTIN-BELL SYNDROME | 2 | 6 |
| 1046 | 7 | 21 | 553 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 |
| 1047 | 4 | 44 | 570 1988 BRAIN AND LANGUAGE 34(2):203-221 VILKMAN E; NIEMI J; IKONEN U FRAGILE-X SPEECH PHONOLOGY IN FINNISH | 5 | 6 |
| 1048 | 0 | 1 | 593 1988 HUMAN GENETICS 80(2):193-193 REKILA AM; VAISANEN ML; KAHKONEN M; LEISTI J; WINQVIST R A NEW RFLP WITH STUI AND PROBE CX55.7 (DXS105) AND ITS USEFULNESS IN CARRIER ANALYSIS OF FRAGILE X-SYNDROME | 2 | 6 |
| 1049 | 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 |
| 1050 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1051 | 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 |
| 1052 | 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 |
| 1053 | 9 | 13 | 939 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):192-196 VERKERK AJMH; DEVRIES BBA; NIERMEIJER MF; FU YH; NELSON DL; et al. INTRAGENIC PROBE USED FOR DIAGNOSTICS IN FRAGILE-X FAMILIES | 5 | 6 |
| 1054 | 18 | 21 | 965 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 44(6):830-833 MALMGREN H; GUSTAVSON KH; WAHLSTROM J; ARPIHENRIKSSON I; BENSCH J; et al. INFANTILE-AUTISM FRAGILE-X - MOLECULAR FINDINGS SUPPORT GENETIC-HETEROGENEITY | 3 | 6 |
| 1055 | 4 | 9 | 1079 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 |
| 1056 | 16 | 28 | 1103 1993 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 35(6):532-539 BARNICOAT AJ; DOCHERTY Z; BOBROW M WHERE HAVE ALL THE FRAGILE-X BOYS GONE | 4 | 6 |
| 1057 | 0 | 1 | 1115 1993 HUMAN MOLECULAR GENETICS 2(8):1348-1348 VERKERK AJMH; DEGRAAFF E; DEBOULLE K; EICHLER EE; KONECKI DS; et al. ALTERNATIVE SPLICING IN THE FRAGILE X-GENE FMR1 (VOL 2, PG 399, 1993) | 3 | 6 |
| 1058 | 8 | 10 | 1194 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):443-446 MINGRONINETTO RC; FERNANDES JG; VIANNAMORGANTE AM RELATIONSHIP OF EXPANSION OF CGG REPEATS AND X-INACTIVATION WITH EXPRESSION OF FRA(X)(Q27.3) IN HETEROZYGOTES | 4 | 6 |
| 1059 | 11 | 13 | 1208 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):501-502 KAPLAN G; KUNG M; MCCLURE M; CRONISTER A DIRECT MUTATION ANALYSIS OF 495 PATIENTS FOR FRAGILE-X CARRIER STATUS PROBAND DIAGNOSIS | 4 | 6 |
| 1060 | 9 | 28 | 1218 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 54(2):141-143 CRADDOCK N; DANIELS J; MCGUFFIN P; OWEN M VARIATION AT THE FRAGILE X-LOCUS DOES NOT INFLUENCE SUSCEPTIBILITY TO BIPOLAR DISORDER | 1 | 6 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1061 | 1 | 2 | 1263 1994 JOURNAL OF MEDICAL GENETICS 31(10):820-820 DEVRIES BBA; NIERMEIJER MF THE PRADER-WILLI-LIKE PHENOTYPE IN FRAGILE-X PATIENTS - A DESIGNATION FACILITATING CLINICAL (AND MOLECULAR) DIFFERENTIAL-DIAGNOSIS | 1 | 6 |
| 1062 | 10 | 25 | 1371 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):327-335 Roy JC; Johnsen J; Breese K; Hagerman R Fragile X syndrome: What is the impact of diagnosis on families? | 3 | 6 |
| 1063 | 2 | 9 | 1390 1995 GENETIC COUNSELING 6(3):207-210 ALEMBIK Y; DOTT B; STOLL C RETT-LIKE SYNDROME IN FRAGILE-X SYNDROME | 1 | 6 |
| 1064 | 27 | 61 | 1427 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 |
| 1065 | 23 | 35 | 1436 1995 PRENATAL DIAGNOSIS 15(9):801-807 CASTELLVIBEL S; MILA M; SOLER A; CARRIO A; SANCHEZ A; et al. PRENATAL-DIAGNOSIS OF FRAGILE-X SYNDROME - (CGG)(N) EXPANSION AND METHYLATION OF CHORIONIC VILLUS SAMPLES | 2 | 6 |
| 1066 | 13 | 17 | 1473 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):270-273 MingroniNetto RC; Haddad LA; ViannaMorgante AM The number of CGG repeats of the FMR1 locus in premutated and fully mutated heterozygotes and their offspring: Implications for the origin of mosaicism | 5 | 6 |
| 1067 | 11 | 28 | 1501 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 |
| 1068 | 20 | 27 | 1528 1996 EUROPEAN JOURNAL OF HUMAN GENETICS 4(1):8-12 Malzac P; Biancalana V; Voelckel MA; Moncla A; Pellissier MC; et al. Unexpected inheritance of the (CGG)(n) trinucleotide expansion in a fragile X syndrome family | 5 | 6 |
| 1069 | 58 | 71 | 1530 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 | 5 | 6 |
| 1070 | 8 | 13 | 1539 1996 HUMAN GENETICS 98(4):419-421 Mila M; CastellviBel S; Gine R; Vazquez C; Badenas C; et al. A female compound heterozygote (pre-and full mutation) for the CGG FMR1 expansion | 4 | 6 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1071 | 3 | 45 | 1560 1996 MEDICAL ANTHROPOLOGY QUARTERLY 10(4):537-550 Nelkin D The social dynamics of genetic testing: The case of Fragile-X | 1 | 6 |
| 1072 | 8 | 27 | 1573 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 | 6 |
| 1073 | 28 | 44 | 1619 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):961-967 Gronskov K; Hjalgrim H; Bjerager MO; BrondumNielsen K Deletion of all CGG repeats plus flanking sequences in FMR1 does not abolish gene expression | 5 | 6 |
| 1074 | 13 | 51 | 1626 1997 AMERICAN JOURNAL OF MEDICAL GENETICS 73(4):463-469 Ritchie RJ; Chakrabarti L; Knight SJL; Harding RM; Davies KE Population genetics of the FRAXE and FRAXF GCC repeats, and a novel CGG repeat, in Xq28 | 2 | 6 |
| 1075 | 1 | 9 | 1645 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 | 6 |
| 1076 | 13 | 28 | 1653 1997 EUROPEAN JOURNAL OF HUMAN GENETICS 5(2):89-93 FulchignoniLataud MC; Olchwang S; Serre JL The fragile X CGG repeat shows a marked level of instability in hereditary non-polyposis colorectal cancer patients | 1 | 6 |
| 1077 | 8 | 11 | 1660 1997 HUMAN GENETICS 99(6):793-795 Chen SH; Schoof JM; Buroker NE; Scott CR The identification of a (CGG)(6)AGG insertion within the CGG repeat of the FMR1 gene in Asians | 5 | 6 |
| 1078 | 7 | 20 | 1694 1997 MOLECULAR DIAGNOSIS 2(4):259-269 Hamdan H; Tynan JA; Fenwick RA; Leon JA Automated detection of trinucleotide repeats in fragile X syndrome | 4 | 6 |
| 1079 | 14 | 22 | 1757 1998 INDIAN JOURNAL OF MEDICAL RESEARCH 107:29-36 Baskaran S; Naseerullah MK; Manjunatha KR; Chetan GK; Arthi R; et al. Triplet repeat polymorphism & fragile X syndrome in the Indian context | 3 | 6 |
| 1080 | 19 | 35 | 1833 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):302-307 Parvari R; Mumm S; Galil A; Manor E; Bar-David Y; et al. Deletion of 8.5 Mb, including the FMR1 gene, in a male with the fragile X syndrome phenotype and overgrowth | 2 | 6 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1081 | 21 | 26 | 1850 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):204-207 Mingroni-Netto RC; Costa SS; Angeli CB; Vianna-Morgante AM DXS548/FRAXAC1 haplotypes in fragile X chromosomes in the Brazilian population | 2 | 6 |
| 1082 | 3 | 6 | 1868 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 | 6 | 6 |
| 1083 | 15 | 19 | 1878 1999 CLINICAL CHEMISTRY AND LABORATORY MEDICINE 37(4):397-401 Houdayer C; Lemonnier A; Gerard M; Chauve C; Tredano M; et al. Improved fluorescent PCR-based assay for sizing CGG repeats at the FRAXA locus | 1 | 6 |
| 1084 | 24 | 33 | 1969 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 93(2):99-106 Larsen LA; Armstrong JSM; Gronskov K; Hjalgrim H; Macpherson JN; et al. Haplotype and AGG-interspersion analysis of FMR1 (CGG)(n) alleles in the Danish population: Implications for multiple mutational pathways towards fragile X alleles | 4 | 6 |
| 1085 | 10 | 14 | 1972 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 95(2):105-107 Tuncbilek E; Alikasifoglu M; Aktas D; Duman F; Yanik H; et al. Screening for the fragile X syndrome among mentally retarded males by hair root analysis | 6 | 6 |
| 1086 | 39 | 66 | 2064 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? | 4 | 6 |
| 1087 | 14 | 42 | 2086 2000 NUCLEIC ACIDS RESEARCH 28(10):2141-2152 Genc B; Muller-Hartmann H; Zeschnigk M; Deissler H; Schmitz B; et al. Methylation mosaicism of 5 '-(CGG)(n)-3 ' repeats in fragile X, premutation and normal individuals | 3 | 6 |
| 1088 | 25 | 49 | 2150 2001 GENETIC EPIDEMIOLOGY 20(1):129-144 Sharma D; Gupta M; Thelma BK Expansion mutation frequency and CGG/GCC repeat polymorphism in FMR1 and FMR2 genes in an Indian population | 4 | 6 |
| 1089 | 1 | 42 | 2152 2001 GENETICS 157(2):717-725 Su MA; Wisotzkey RG; Newfeld SJ A screen for modifiers of decapentaplegic mutant phenotypes identifies lilliputian, the only member of the Fragile-X/Burkitt's lymphoma family of transcription factors in Drosophila melanogaster | 0 | 6 |
| 1090 | 35 | 47 | 2155 2001 HUMAN GENETICS 108(6):450-458 Weinhausel A; Haas OA Evaluation of the fragile X (FRAXA) syndrome with methylation-sensitive PCR | 2 | 6 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1091 | 19 | 31 | 2162 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 |
| 1092 | 13 | 27 | 2214 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 | 6 |
| 1093 | 12 | 24 | 2251 2002 BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 292(4):1063-1069 Denman RB; Sung YJ Species-specific and isoform-specific RNA binding of human and mouse fragile X mental retardation proteins | 6 | 6 |
| 1094 | 7 | 21 | 2254 2002 CELLULAR & MOLECULAR BIOLOGY LETTERS 7(3):877-883 Denman RB Methylation of the arginine-glycine-rich region in the fragile X mental retardation protein FMRP differentially affects RNA binding | 2 | 6 |
| 1095 | 17 | 25 | 2261 2002 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 44(11):724-728 Berry-Kravis E Epilepsy in fragile X syndrome | 5 | 6 |
| 1096 | 0 | 53 | 2292 2002 JOURNAL OF BACTERIOLOGY 184(1):177-182 Semsey S; Blaha B; Koles K; Orosz L; Papp PP Site-specific integrative elements of rhizobiophage 16-3 can integrate into proline tRNA (CGG) genes in different bacterial genera | 1 | 6 |
| 1097 | 32 | 51 | 2298 2002 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 23(6):416-423 Loesch DZ; Huggins RM; Bui QM; Epstein JL; Taylor AK; et al. Effect of the deficits of fragile X mental retardation protein on cognitive status of fragile X males and females assessed by robust pedigree analysis | 6 | 6 |
| 1098 | 13 | 25 | 2305 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; et al. Genetic and environmental influences on the cognitive outcomes of children with fragile X syndrome | 6 | 6 |
| 1099 | 20 | 42 | 2313 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 | 6 |
| 1100 | 23 | 52 | 2342 2002 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 99(24):15758-15763 Qin M; Kang J; Smith CB Increased rates of cerebral glucose metabolism in a mouse model of fragile X mental retardation | 5 | 6 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1101 | 15 | 28 | 2377 2003 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 117A(1):21-29 Glaser B; Hessl D; Dyer-Friedman J; Johnston C; Wisbeck J; et al. Biological and environmental contributions to adaptive behavior in fragile X syndrome | 0 | 6 |
| 1102 | 29 | 58 | 2382 2003 AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS 118B(1):81-88 Barnea-Goraly N; Eliez S; Hedeus M; Menon V; White CD; et al. White matter tract alterations in fragile X syndrome: Preliminary evidence from diffusion tensor imaging | 0 | 6 |
| 1103 | 13 | 41 | 2405 2003 BRAIN RESEARCH 971(1):83-89 Galvez R; Gopal AR; Greenough WT Somatosensory cortical barrel dendritic abnormalities in a mouse model of the fragile X mental retardation syndrome | 4 | 6 |
| 1104 | 20 | 54 | 2436 2003 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 33(1):55-67 Lesniak-Karpiak K; Mazzocco MMM; Ross JL Behavioral assessment of social anxiety in females with Turner or fragile X syndrome | 0 | 6 |
| 1105 | 8 | 36 | 2470 2003 PEDIATRICS 111(2):407-416 Bailey DB; Skinner D; Sparkman KL Discovering fragile X syndrome: Family experiences and perceptions | 5 | 6 |
| 1106 | 0 | 21 | 2474 2003 PROTEIN EXPRESSION AND PURIFICATION 27(2):365-374 McNulty DE; Claffee BA; Huddleston MJ; Kane JF Mistranslational errors associated with the rare arginine codon CGG in Escherichia coli | 1 | 6 |
| 1107 | 13 | 32 | 2529 2004 HUMAN MOLECULAR GENETICS 13(5):543-549 Beilina A; Tassone F; Schwartz PH; Sahota P; Hagerman PJ Redistribution of transcription start sites within the FMR1 promoter region with expansion of the downstream CGG-repeat element | 4 | 6 |
| 1108 | 0 | 3 | 46 1982 AMERICAN JOURNAL OF HUMAN GENETICS 34(6):A129-A129 HOWARDPEEBLES PN FRAGILE X-CHROMOSOME - THE ROLE OF METHIONINE AND OTHER INVITRO MANIPULATIONS | 4 | 5 |
| 1109 | 0 | 0 | 81 1982 LANCET 2(8307):1104-1104 KINNELL HG FRAGILE-X DISORDER ASSOCIATED WITH ANTISOCIAL PERSONALITY | 3 | 5 |
| 1110 | 0 | 0 | 97 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A131-A131 EREN M; DISTECHE C BEHAVIORAL-PHENOTYPE OF THE FRAGILE X-SYNDROME - RELATIONSHIP BETWEEN FREQUENCY OF MARKER-X, MENTAL-RETARDATION AND VERBAL DISABILITY | 3 | 5 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1111 | 2 | 11 | 182 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):255-257 DANIEL A; EKBLOM L; PHILLIPS S FRAGILE-X EXPRESSION SUPPRESSED IN EITHER FUDR OR METHOTREXATE TREATED FIBROBLASTS BY PRETREATMENT WITH 5-AZACYTIDINE | 3 | 5 |
| 1112 | 3 | 6 | 208 1984 HUMAN GENETICS 68(4):346-347 DEARCE MA VERIFICATION OF LYONS HYPOTHESIS IN FRAGILE-X CARRIERS | 2 | 5 |
| 1113 | 6 | 17 | 242 1985 AMERICAN JOURNAL OF HUMAN GENETICS 37(1):193-198 ABRUZZO MA; MAYER M; JACOBS PA THE EFFECT OF METHIONINE AND 5-AZACYTIDINE ON FRAGILE-X EXPRESSION | 3 | 5 |
| 1114 | 4 | 18 | 245 1985 AMERICAN JOURNAL OF HUMAN GENETICS 37(5):947-955 CANTU ES; NUSSBAUM RL; AIRHART SD; LEDBETTER DH FRAGILE (X) EXPRESSION INDUCED BY FUDR IS TRANSIENT AND INVERSELY RELATED TO LEVELS OF THYMIDYLATE SYNTHASE ACTIVITY | 3 | 5 |
| 1115 | 1 | 12 | 248 1985 AMERICAN JOURNAL OF MEDICAL GENETICS 21(4):691-696 WANG JCC; BEARDSLEY GP; ERBE RW ANTIFOLATE-INDUCED MISINCORPORATION OF DEOXYURIDINE MONOPHOSPHATE INTO DNA BY CELLS FROM PATIENTS WITH THE FRAGILE-X SYNDROME | 2 | 5 |
| 1116 | 4 | 11 | 269 1985 CLINICAL GENETICS 28(2):97-99 ABUELO D; CASTREE K; PUESCHEL S; PADREMENDOZA T; ZOLNIERZ K FREQUENCY OF FRAGILE X-CHROMOSOME IN NORMAL FEMALES | 2 | 5 |
| 1117 | 0 | 0 | 277 1985 CYTOGENETICS AND CELL GENETICS 40(1-4):715-715 OBERLE I; ARVEILER B; MATTEI MG; MATTEI JF; BOUE J; et al. LINKAGE ANALYSIS OF THE FRAGILE X-MENTAL RETARDATION SYNDROME WITH FLANKING POLYMORPHIC DNA MARKERS | 2 | 5 |
| 1118 | 4 | 15 | 313 1985 SOMATIC CELL AND MOLECULAR GENETICS 11(4):353-357 WANG JCC; ERBE RW THYMIDYLATE METABOLISM IN FRAGILE-X SYNDROME CELLS | 3 | 5 |
| 1119 | 6 | 12 | 332 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):291-296 WELLS TE; MADISON LS ASSESSMENT OF BEHAVIOR-CHANGE IN A FRAGILE-X SYNDROME MALE TREATED WITH FOLIC-ACID | 3 | 5 |
| 1120 | 3 | 7 | 347 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):531-535 JENKINS EC; DUNCAN CJ; KRAWCZUN MS; BERNS LM; SANZ MM; et al. FREQUENCY OF TRIRADIAL OR MULTIRADIAL CONFIGURATIONS IN FRAGILE-X IDENTIFICATION | 3 | 5 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1121 | 2 | 4 | 434 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 |
| 1122 | 8 | 14 | 456 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 |
| 1123 | 1 | 2 | 487 1987 LANCET 2(8554):329-329 VERLOES A; SACRE JP; GEUBELLE F SOTOS SYNDROME AND FRAGILE-X CHROMOSOMES | 1 | 5 |
| 1124 | 8 | 20 | 515 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 |
| 1125 | 1 | 2 | 537 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 |
| 1126 | 2 | 29 | 573 1988 CHROMOSOMA 97(1):6-10 KEREM B; GOITEIN R; SCHAAP T CYTOLOGICAL EVIDENCE OF DEFECTIVE TEMPLATE IN THE FRAGILE X-CHROMOSOME | 2 | 5 |
| 1127 | 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 |
| 1128 | 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 |
| 1129 | 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 |
| 1130 | 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 |
| 1131 | 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 |
| 1132 | 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 |
| 1133 | 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 |
| 1134 | 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 |
| 1135 | 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 |
| 1136 | 3 | 12 | 890 1991 NATURE 349(6312):742-743 CRAIG I HUMAN-GENETICS - METHYLATION AND THE FRAGILE-X | 1 | 5 |
| 1137 | 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 |
| 1138 | 1 | 16 | 928 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):124-127 TIROSH E; BOROCHOWITZ Z SLEEP-APNEA IN FRAGILE-X SYNDROME | 3 | 5 |
| 1139 | 4 | 14 | 966 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 |
| 1140 | 18 | 33 | 1020 1992 PEDIATRIC NEUROLOGY 8(4):272-274 WONG VCN; LAM STS FRAGILE X POSITIVITY IN CHINESE CHILDREN WITH AUTISTIC SPECTRUM DISORDER | 3 | 5 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1141 | 12 | 15 | 1078 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 |
| 1142 | 1 | 8 | 1089 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 |
| 1143 | 16 | 20 | 1097 1993 CLINICAL GENETICS 44(4):169-172 YAMAUCHI M; NAGATA S; SEKI N; TOYAMA Y; HARADA N; et al. PRENATAL-DIAGNOSIS OF FRAGILE X-SYNDROME BY DIRECT-DETECTION OF THE DYNAMIC MUTATION DUE TO AN UNSTABLE DNA-SEQUENCE | 2 | 5 |
| 1144 | 14 | 31 | 1109 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 |
| 1145 | 7 | 9 | 1137 1993 JOURNAL OF MEDICAL GENETICS 30(9):785-787 SUZUMORI K; YAMAUCHI M; SEKI N; KONDO I; HORI T PRENATAL-DIAGNOSIS OF A HYPERMETHYLATED FULL FRAGILE-X MUTATION IN CHORIONIC VILLI OF A MALE FETUS | 1 | 5 |
| 1146 | 17 | 34 | 1146 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 |
| 1147 | 4 | 8 | 1272 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 |
| 1148 | 18 | 19 | 1331 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 |
| 1149 | 40 | 112 | 1342 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 |
| 1150 | 4 | 9 | 1481 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):319-322 Fisch GS; Carpenter N; Maddalena A; Tarleton J; JulienInalsingh C; et al. Rater reliability of fragile X mutation size estimates: A multilaboratory analysis | 5 | 5 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1151 | 4 | 13 | 1509 1996 ARCHIVES OF MEDICAL RESEARCH 27(4):587-588 Rivera H Fragile X studies and authorship | 1 | 5 |
| 1152 | 0 | 12 | 1515 1996 BRITISH JOURNAL OF HAEMATOLOGY 93(4):841-844 Arjona SN; EloyGarcia J; Gu LH; Smetanina NS; Huisman THJ The dominant beta-thalassaemia in a Spanish family is due to a frameshift that introduces an extra CGG codon (=arginine) at the 5' end of the second exon | 0 | 5 |
| 1153 | 3 | 14 | 1622 1997 AMERICAN JOURNAL OF MEDICAL GENETICS 68(4):445-449 Wen GY; Jenkins EC; Yao XL; Yoon D; Brown WT; et al. Transmission electron microscopy of chromosomes by longitudinal section preparation: Application to fragile X chromosome analysis | 3 | 5 |
| 1154 | 5 | 8 | 1658 1997 HOSPITAL PRACTICE 32(4):73-& Warren ST Trinucleotide repetition and fragile X syndrome | 3 | 5 |
| 1155 | 12 | 28 | 1726 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 |
| 1156 | 21 | 29 | 1750 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 |
| 1157 | 2 | 4 | 1754 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 |
| 1158 | 1 | 38 | 1767 1998 JOURNAL OF BIOLOGICAL CHEMISTRY 273(46):30466-30471 Mangel L; Ternes T; Schmitz B; Doerfler W New 5 '-(CGG)(n)-3 ' repeats in the human genome | 3 | 5 |
| 1159 | 3 | 35 | 1775 1998 JOURNAL OF INTERFERON AND CYTOKINE RESEARCH 18(8):609-616 Xu Z; Williams BRG Genomic features of human PKR: Alternative splicing and a polymorphic CGG repeat in the 5 '-untranslated region | 0 | 5 |
| 1160 | 0 | 26 | 1793 1998 NUCLEIC ACIDS RESEARCH 26(12):3001-3005 Dutta R; Gao YG; Priebe W; Wang AHJ Binding of the modified daunorubicin WP401 adjacent to a T-G base pair induces the reverse Watson-Crick conformation: crystal structures of the WP401-TGGCCG and WP401-CGG[br(5)C]CG complexes | 0 | 5 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1161 | 3 | 7 | 1844 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):350-351 Faradz SMH; Buckley M; Tang LP; Leigh D; Holden JJA Molecular screening for fragile X syndrome among Indonesian children with developmental disability | 3 | 5 |
| 1162 | 10 | 14 | 1851 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):214-216 Pekarik V; Blazkova M; Kozak L Haplotype analysis of the fragile X syndrome gene FMR1 in the Czech Republic | 2 | 5 |
| 1163 | 15 | 23 | 1859 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 | 4 | 5 |
| 1164 | 4 | 36 | 1860 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):272-276 Currie JR; Brown WT KH domain-containing proteins of yeast: Absence of a fragile X gene homologue | 0 | 5 |
| 1165 | 21 | 34 | 1891 1999 EUROPEAN JOURNAL OF HUMAN GENETICS 7(7):771-777 Larsen LA; Armstrong JSM; Gronskov K; Hjalgrim H; Brondum-Nielsen K; et al. Analysis of FMR1 (CGG)(n) alleles and FRAXA microsatellite haplotypes in the population of Greenland: implications for the population of the New World from Asia | 3 | 5 |
| 1166 | 0 | 28 | 1892 1999 EXPERIMENTAL CELL RESEARCH 251(2):388-400 Yano H; Wang BE; Ahmad I; Zhang JZ; Abo T; et al. Identification of (CAG)(n) and (CGG)(n) repeat-binding proteins, CAGERs expressed in mature neurons of the mouse brain | 0 | 5 |
| 1167 | 37 | 57 | 1898 1999 HUMAN BIOLOGY 71(1):55-68 Arrieta I; Gil A; Nunez T; Telez M; Martinez B; et al. Stability of the FMRI CGG repeat in a Basque sample | 4 | 5 |
| 1168 | 63 | 96 | 1906 1999 INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE 3(6):639-645 Pimentel MMG Fragile X syndrome | 0 | 5 |
| 1169 | 18 | 28 | 1921 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 |
| 1170 | 4 | 4 | 1923 1999 LANCET 353(9159):1153-1154 Hong CJ; Song HL; Lai HC; Tsai SJ; Hsiao KJ Methanol/acetone treatment helps the amplification of FMR1 CGG repeat fragment in dried blood spots from Guthrie cards | 1 | 5 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1171 | 1 | 1 | 1930 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 |
| 1172 | 3 | 3 | 1941 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 |
| 1173 | 24 | 33 | 2001 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 |
| 1174 | 21 | 36 | 2062 2000 JOURNAL OF MEDICAL GENETICS 37(1):77-79 Beresford RG; Tatlidil C; Riddell DC; Welch JP; Ludman MD; et al. Absence of fragile X syndrome in Nova Scotia | 4 | 5 |
| 1175 | 22 | 29 | 2072 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 |
| 1176 | 12 | 20 | 2075 2000 MOLECULAR AND CELLULAR PROBES 14(2):115-119 Mila M; Castellvi-Bel S; Sanchez A; Barcelo A; Badenas C; et al. Rare variants in the promoter of the fragile X syndrome gene (FMR1) | 5 | 5 |
| 1177 | 18 | 39 | 2325 2002 NEUROBIOLOGY OF DISEASE 11(1):53-63 Schenck A; Van de Bor V; Bardoni B; Giangrande A Novel features of dFMR1, the Drosophila orthologue of the fragile X mental retardation protein | 4 | 5 |
| 1178 | 20 | 41 | 2379 2003 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 118A(2):127-134 Loesch DZ; Huggins RM; Bui QM; Taylor AK; Hagerman RJ Relationship of deficits of FMR1 gene specific protein with physical phenotype of fragile X males and females in pedigrees: A new perspective | 0 | 5 |
| 1179 | 35 | 62 | 2380 2003 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 122A(1):13-23 Loesch DZ; Huggins RM; Bui QM; Taylor AK; Pratt C; et al. Effect of fragile x status categories and FMRP deficits on cognitive profiles estimated by robust pedigree analysis | 0 | 5 |
| 1180 | 15 | 39 | 2385 2003 AMERICAN JOURNAL ON MENTAL RETARDATION 108(3):149-160 Abbeduto L; Murphy MM; Cawthon SW; Richmond EK; Weissman MD; et al. Receptive language skills of adolescents and young adults with Down or fragile X syndrome | 2 | 5 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1181 | 69 | 87 | 2411 2003 CURRENT OPINION IN PEDIATRICS 15(6):559-566 Chiurazzi P; Neri G; Oostra BA Understanding the biological underpinnings of fragile X syndrome | 2 | 5 |
| 1182 | 97 | 168 | 2413 2003 CYTOGENETIC AND GENOME RESEARCH 100(1-4):111-123 Bakker CE; Oostra BA Understanding fragile X syndrome: insights from animal models | 4 | 5 |
| 1183 | 21 | 50 | 2468 2003 NUCLEIC ACIDS RESEARCH 31(14):3963-3970 Weisman-Shomer P; Cohen E; Hershco I; Khateb S; Wolfovitz-Barchad O; et al. The cationic porphyrin TMPyP4 destabilizes the tetraplex form of the fragile X syndrome expanded sequence d(CGG)(n) | 3 | 5 |
| 1184 | 42 | 102 | 2575 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):60-67 Willemsen R; Oostra BA; Bassell GJ; Dictenberg J The fragile X syndrome: From molecular genetics to neurobiology | 2 | 5 |
| 1185 | 24 | 40 | 2603 2004 NUCLEIC ACIDS RESEARCH 32(7):2129-2137 Gabus C; Mazroui R; Tremblay S; Khandjian EW; Darlix JL The fragile X mental retardation protein has nucleic acid chaperone properties | 2 | 5 |
| 1186 | 0 | 3 | 47 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 |
| 1187 | 0 | 0 | 93 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A92-A92 HAGERMAN R; MCBOGG P; LEVITUS A; MCGAVRAN L; SMITH A; et al. FOLIC-ACID TREATMENT OF THE FRAGILE-X SYNDROME | 3 | 4 |
| 1188 | 0 | 0 | 99 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A136-A136 JENKINS E; DUNCAN C; BROOKS J; LELE K; SANZ M; et al. LOW-FREQUENCY FRAGILE X-CHROMOSOMES IN CULTURES FROM NORMAL PEOPLE | 0 | 4 |
| 1189 | 4 | 5 | 109 1983 AMERICAN JOURNAL OF MEDICAL GENETICS 14(4):795-796 DAKER MG FRAGILE X-CHROMOSOME IN NORMAL MALES | 2 | 4 |
| 1190 | 2 | 15 | 115 1983 ANNALES DE GENETIQUE 26(3):171-173 JACKY PB; DILL FJ FRAGILE-X CHROMOSOME AND CHROMOSOME CONDENSATION | 1 | 4 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1191 | 3 | 9 | 140 1983 HUMAN GENETICS 65(1):88-89 SOUDEK D; EMANUEL M A FRAGILE X SUPPRESSOR IN THE NORMAL HUMAN-BLOOD | 3 | 4 |
| 1192 | 3 | 8 | 162 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 |
| 1193 | 0 | 0 | 203 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 |
| 1194 | 1 | 3 | 217 1984 JOURNAL OF MEDICAL GENETICS 21(1):74-75 SUTHERLAND GR ROUTINE DIAGNOSTIC-DETECTION OF THE FRAGILE X | 1 | 4 |
| 1195 | 1 | 4 | 224 1984 LANCET 1(8370):220-220 WEBB T; THAKE A; TODD J; BUNDEY S PREVALENCE OF FRAGILE X-CHROMOSOME | 2 | 4 |
| 1196 | 0 | 4 | 226 1984 LANCET 1(8370):220-221 LINNA SL; SIMILA S; HARO E; HERVA R PREVALENCE OF FRAGILE X-CHROMOSOME | 2 | 4 |
| 1197 | 3 | 6 | 235 1984 PRENATAL DIAGNOSIS 4(6):473-474 VENTER PA; COETZEE DJ; BADENHORST A; MARX MP; HOF JO; et al. A CONFIRMED PRENATAL-DIAGNOSIS OF A FEMALE FETUS WITH THE FRAGILE X-CHROMOSOME | 1 | 4 |
| 1198 | 0 | 3 | 260 1985 CANADIAN MEDICAL ASSOCIATION JOURNAL 133(5):358-& SOUDEK D FRAGILE-X - A SYMPTOM OF THE DISEASE | 2 | 4 |
| 1199 | 0 | 0 | 265 1985 CLINICAL GENETICS 27(3):334-335 SCHMIDT A PRENATAL-DIAGNOSIS OF FRAGILE X-SYNDROME | 2 | 4 |
| 1200 | 0 | 4 | 278 1985 CYTOGENETICS AND CELL GENETICS 40(1-4):726-726 PURRELLO M; ALHADEFF B; ROCCHI M; ARCHIDIACONO N; DRAYNA D; et al. 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 |