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Nodes: 2647,
Authors: 5321,
Journals: 428,
Outer References: 16458,
Words: 3536
Collection span: 1967 - 2005
View: Overview. Sorted by LCS.
Page 4: 1 2 3 4 5 6 7 8 9
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 901 | 66 | 100 | 2139 2001 CLINICAL GENETICS 60(6):399-408 Oostra BA; Chiurazzi P The fragile X gene and its function | 5 | 11 |
| 902 | 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 |
| 903 | 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 |
| 904 | 17 | 25 | 2261 2002 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 44(11):724-728 Berry-Kravis E Epilepsy in fragile X syndrome | 5 | 6 |
| 905 | 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 |
| 906 | 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 |
| 907 | 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 |
| 908 | 2 | 4 | 19 1981 CLINICAL GENETICS 20(1):78-78 HOWARDPEEBLES PN FRAGILE-X CHROMOSOME IN NORMAL MALES | 4 | 7 |
| 909 | 0 | 9 | 27 1981 LANCET 1(8219):557-557 EBERLE G; ZANKL H; ZANKL M SOURCES OF ERROR IN FRAGILE-X DETERMINATION | 4 | 8 |
| 910 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 911 | 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 |
| 912 | 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 |
| 913 | 3 | 20 | 183 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):259-273 HOLDEN JJA; WANG HS; WHITE BN THE FRAGILE-X SYNDROME .4. PROGRESS TOWARDS THE IDENTIFICATION OF LINKED RESTRICTION FRAGMENT LENGTH VARIANTS (RFLVS) | 4 | 13 |
| 914 | 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 |
| 915 | 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 |
| 916 | 3 | 24 | 206 1984 HUMAN GENETICS 67(1):99-102 CANTU ES; JACOBS PA FRAGILE (X) EXPRESSION - RELATIONSHIP TO THE CELL-CYCLE | 4 | 7 |
| 917 | 2 | 8 | 216 1984 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 5(4):201-203 KERBESHIAN J; BURD L; MARTSOLF JT FRAGILE X-SYNDROME ASSOCIATED WITH TOURETTE SYMPTOMATOLOGY IN A MALE WITH MODERATE MENTAL-RETARDATION AND AUTISM | 4 | 29 |
| 918 | 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 |
| 919 | 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 |
| 920 | 1 | 9 | 285 1985 HUMAN GENETICS 69(3):206-208 MAYER M; ABRUZZO MA; JACOBS PA; YEE SC A CYTOGENETIC STUDY OF A POPULATION OF RETARDED FEMALES WITH SPECIAL REFERENCE TO THE FRAGILE (X) SYNDROME | 4 | 10 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 921 | 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 |
| 922 | 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 |
| 923 | 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 |
| 924 | 0 | 0 | 363 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 |
| 925 | 9 | 45 | 385 1986 COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY 51:195-203 MANDEL JL; ARVEILER B; CAMERINO G; HANAUER A; HEILIG R; et al. GENETIC-MAPPING OF THE HUMAN X-CHROMOSOME - LINKAGE ANALYSIS OF THE Q26-Q28 REGION THAT INCLUDES THE FRAGILE X-LOCUS AND ISOLATION OF EXPRESSED SEQUENCES | 4 | 36 |
| 926 | 6 | 10 | 422 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 |
| 927 | 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 |
| 928 | 1 | 2 | 528 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):237-238 EINFELD SL AUTISM AND THE FRAGILE-X SYNDROME | 4 | 6 |
| 929 | 16 | 23 | 534 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):393-399 FISCH GS; COHEN IL; GROSS AC; JENKINS V; JENKINS EC; et al. FOLIC-ACID TREATMENT OF FRAGILE-X MALES - A FURTHER STUDY | 4 | 9 |
| 930 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 931 | 14 | 27 | 542 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):531-542 SCHWARTZ CE; PHELAN MC; BRIGHTHARP C; PANCOAST I; HOWARDPEEBLES PN; et al. FRAGILE-X SYNDROME - LINKAGE ANALYSIS IN BLACK AND WHITE-POPULATIONS | 4 | 4 |
| 932 | 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 |
| 933 | 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 |
| 934 | 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 |
| 935 | 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 |
| 936 | 4 | 22 | 646 1989 HUMAN GENETICS 81(4):377-381 TOMMERUP N INDUCTION OF THE FRAGILE X ON BRDU-SUBSTITUTED CHROMOSOMES WITH DIRECT VISUALIZATION OF SISTER CHROMATID EXCHANGES ON BANDED CHROMOSOMES | 4 | 4 |
| 937 | 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 |
| 938 | 9 | 16 | 685 1990 AMERICAN JOURNAL OF MEDICAL GENETICS 36(1):122-125 VANROY BC; WILLEMS PJ; VITS LJ; CEULEMANS BP; COUCKE PJ; et al. 2 BROTHERS WITH MENTAL-RETARDATION DISCORDANT FOR THE FRAGILE-X SYNDROME | 4 | 4 |
| 939 | 5 | 14 | 707 1990 HUMAN GENETICS 84(3):263-266 ROUSSEAU F; VINCENT A; OBERLE I; MANDEL JL NEW INFORMATIVE POLYMORPHISM AT THE DXS304 LOCUS, A CLOSE DISTAL MARKER FOR THE FRAGILE X-LOCUS | 4 | 19 |
| 940 | 12 | 23 | 795 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):292-297 BROWN WT; GROSS A; GOONEWARDENA P; FERRANDO C; DOBKIN C; et al. DETECTION OF FRAGILE-X NON-PENETRANT MALES BY DNA MARKER ANALYSIS | 4 | 4 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 941 | 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 |
| 942 | 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 |
| 943 | 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 |
| 944 | 7 | 16 | 868 1991 HUMAN GENETICS 87(3):369-372 HULSEBOS TJM; OOSTRA BA; BROERSEN S; SMITS A; VANOOST BA; et al. NEW DISTAL MARKER CLOSELY LINKED TO THE FRAGILE-X LOCUS | 4 | 13 |
| 945 | 5 | 11 | 924 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):96-102 BROWN WT; JENKINS EC; GOONEWARDENA P; MIEZEJESKI C; ATKIN J; et al. PRENATALLY DETECTED FRAGILE-X FEMALES - LONG-TERM FOLLOW-UP-STUDIES SHOW HIGH-RISK OF MENTAL IMPAIRMENT | 4 | 4 |
| 946 | 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 |
| 947 | 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 |
| 948 | 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 |
| 949 | 8 | 14 | 1031 1993 AMERICAN JOURNAL OF DISEASES OF CHILDREN 147(6):605-606 GOLDSON E; HAGERMAN RJ FRAGILE-X SYNDROME AND FAILURE-TO-THRIVE | 4 | 4 |
| 950 | 5 | 17 | 1087 1993 BIOLOGICAL PSYCHIATRY 33(3):213-216 JEFFRIES FM; REISS AL; BROWN WT; MEYERS DA; GLICKSMAN AC; et al. BIPOLAR SPECTRUM DISORDER AND FRAGILE-X SYNDROME - A FAMILY STUDY | 4 | 13 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 951 | 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 |
| 952 | 17 | 34 | 1098 1993 CURRENT BIOLOGY 3(11):783-786 TROTTIER Y; DEVYS D; MANDEL JL FRAGILE-X SYNDROME - AN EXPANDING STORY | 4 | 8 |
| 953 | 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 |
| 954 | 7 | 23 | 1129 1993 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 37:131-142 BUTLER MG; SINGH DN CLINICAL AND CYTOGENETIC SURVEY OF INSTITUTIONALIZED MENTALLY-RETARDED PATIENTS WITH EMPHASIS ON THE FRAGILE-X SYNDROME | 4 | 9 |
| 955 | 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 |
| 956 | 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 |
| 957 | 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 |
| 958 | 10 | 23 | 1230 1994 CLINICAL GENETICS 45(4):175-180 SCHRANDERSTUMPEL C; GERVER WJ; MEYER H; ENGELEN J; MULDER H; et al. PRADER-WILLI-LIKE PHENOTYPE IN FRAGILE-X SYNDROME | 4 | 17 |
| 959 | 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 |
| 960 | 46 | 131 | 1360 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):199-217 Binstock TC Fragile X and the amygdala: Cognitive, interpersonal, emotional, and neuroendocrine considerations | 4 | 4 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 961 | 21 | 43 | 1434 1995 PEDIATRIC RESEARCH 38(5):638-643 BERRYKRAVIS E; HICAR M; CIURLIONIS R REDUCED CYCLIC-AMP PRODUCTION IN FRAGILE-X SYNDROME - CYTOGENETIC AND MOLECULAR CORRELATIONS | 4 | 4 |
| 962 | 42 | 70 | 1439 1995 SEMINARS IN CELL BIOLOGY 6(1):5-11 NELSON DL THE FRAGILE-X SYNDROMES | 4 | 16 |
| 963 | 12 | 81 | 1511 1996 BIOCHEMISTRY 35(15):5041-5053 Pearson CE; Sinden RR Alternative structures in duplex DNA formed within the trinucleotide repeats of the myotonic dystrophy and fragile X loci | 4 | 91 |
| 964 | 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 |
| 965 | 6 | 37 | 1547 1996 JOURNAL OF BIOLOGICAL CHEMISTRY 271(38):22937-22940 Wang YH; Griffith J Methylation of expanded CCG triplet repeat DNA from fragile X syndrome patients enhances nucleosome exclusion | 4 | 23 |
| 966 | 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 |
| 967 | 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 |
| 968 | 16 | 23 | 1664 1997 HUMAN GENETICS 101(2):214-218 Hirst MC; Arinami T; Laird CD Sequence analysis of long FMR1 arrays in the Japanese population: insights into the generation of long (CGG)(n) tracts | 4 | 9 |
| 969 | 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 |
| 970 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 971 | 10 | 39 | 1760 1998 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 28(4):321-328 Mazzocco MMM; Pulsifer M; Fiumara A; Cocuzza M; Nigro F; et al. Brief report: Autistic behaviors among children with fragile X or Rett syndrome: Implications for the classification of pervasive developmental disorder | 4 | 9 |
| 972 | 11 | 33 | 1768 1998 JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS 15(4):745-756 Chen X; Mariappan SVS; Moyzis RK; Bradbury EM; Gupta G Hairpin induced slippage and hyper-methylation of the fragile X DNA triplets | 4 | 16 |
| 973 | 7 | 40 | 1769 1998 JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY AND ALLIED DISCIPLINES 39(5):699-710 van Lieshout CFM; De Meyer RE; Curfs LMG; Fryns JP Family contexts, parental behaviour, and personality profiles of children and adolescents with Prader-Willi, fragile-X, or Williams syndrome | 4 | 16 |
| 974 | 8 | 39 | 1783 1998 JOURNAL OF MOLECULAR BIOLOGY 283(1):111-120 Mariappan SVS; Silks LA; Bradbury EM; Gupta G Fragile X DNA triplet repeats, (GCC)(n), form hairpins with single hydrogen-bonded cytosine center dot cytosine mispairs at the CpG sites: Isotope-edited nuclear magnetic resonance spectroscopy on (GCC)(n) with selective (15)N4-labeled cytosine bases | 4 | 18 |
| 975 | 11 | 14 | 1843 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):347-349 Chiurazzi P; Pomponi MG; Sharrock A; Macpherson J; Lormeau S; et al. DNA panel for interlaboratory standardization of haplotype studies on the fragile X syndrome and proposal for a new allele nomenclature | 4 | 11 |
| 976 | 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 |
| 977 | 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 |
| 978 | 22 | 38 | 1871 1999 ANNALES DE GENETIQUE 42(4):197-201 Arrieta I; Criado B; Martinez B; Telez M; Nunez T; et al. A survey of fragile X syndrome in a sample from Spanish Basque country | 4 | 4 |
| 979 | 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 |
| 980 | 16 | 22 | 1919 1999 JOURNAL OF MEDICAL GENETICS 36(6):467-470 de Vries BBA; Mohkamsing S; van den Ouweland AMW; Mol E; Gelsema K; et al. Screening for the fragile X syndrome among the mentally retarded: a clinical study | 4 | 12 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 981 | 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 |
| 982 | 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 |
| 983 | 4 | 46 | 1990 2000 BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 278(3):833-838 Patel PK; Bhavesh NS; Hosur RV Cation-dependent conformational switches in d-TGGCGGC containing two triplet repeats of Fragile X Syndrome: NMR observations | 4 | 9 |
| 984 | 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 |
| 985 | 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 |
| 986 | 21 | 34 | 2095 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(3):504-515 Wohrle D; Salat U; Hameister H; Vogel W; Steinbach P Demethylation, reactivation, and destabilization of human fragile X full-mutation alleles in mouse embryocarcinoma cells | 4 | 10 |
| 987 | 20 | 55 | 2115 2001 AMERICAN JOURNAL OF MEDICAL GENETICS 103(1):81-90 Sun HT; Cohen S; Kaufmann WE Annexin-1 is abnormally expressed in fragile X syndrome: Two-dimensional electrophoresis study in lymphocytes | 4 | 9 |
| 988 | 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 |
| 989 | 15 | 58 | 2165 2001 JOURNAL OF BIOLOGICAL CHEMISTRY 276(19):16439-16446 Kamath-Loeb AS; Loeb LA; Johansson E; Burgers PMJ; Fry M Interactions between the Werner syndrome helicase and DNA polymerase delta specifically facilitate copying of tetraplex and hairpin structures of the d(CGG)(n) trinucleotide repeat sequence | 4 | 44 |
| 990 | 10 | 13 | 2213 2001 SCIENCE 294(5551):2487-2488 Moine H; Mandel JL Biomedicine - Do G quartets orchestrate fragile X pathology? | 4 | 9 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 991 | 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 |
| 992 | 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 |
| 993 | 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 |
| 994 | 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 |
| 995 | 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 |
| 996 | 40 | 52 | 2431 2003 HUMAN MOLECULAR GENETICS 12(23):3087-3096 Mazroui R; Huot ME; Tremblay S; Boilard N; Labelle Y; et al. Fragile X Mental Retardation protein determinants required for its association with polyribosomal mRNPs | 4 | 4 |
| 997 | 27 | 61 | 2456 2003 MOLECULAR BRAIN RESEARCH 110(2):267-278 Todd PK; Malter JS; Mack KJ Whisker stimulation-dependent translation of FMRP in the barrel cortex requires activation of type I metabotropic glutamate receptors | 4 | 3 |
| 998 | 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 |
| 999 | 0 | 0 | 9 1981 AMERICAN JOURNAL OF HUMAN GENETICS 33(6):A99-A99 BRYANT EM; HOEHN H; MARTIN GM EXPRESSION OF THE FRAGILE X IN EUPLOID SOMATIC-CELL HYBRIDS | 3 | 3 |
| 1000 | 0 | 0 | 41 1982 AMERICAN JOURNAL OF HUMAN GENETICS 34(6):A82-A82 BROWN T; JENKINS E; FRIEDMAN E; BROOKS J; DUNCAN C; et al. A CONTROLLED TRIAL OF FOLIC-ACID THERAPY IN FRAGILE-X INDIVIDUALS | 3 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1001 | 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 |
| 1002 | 16 | 81 | 53 1982 ARCHIVES FRANCAISES DE PEDIATRIE 39(8):633-639 MATTEI JF FRAGILE X-LINKED MENTAL-RETARDATION | 3 | 3 |
| 1003 | 0 | 0 | 81 1982 LANCET 2(8307):1104-1104 KINNELL HG FRAGILE-X DISORDER ASSOCIATED WITH ANTISOCIAL PERSONALITY | 3 | 5 |
| 1004 | 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 |
| 1005 | 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 |
| 1006 | 1 | 1 | 121 1983 CLINICAL GENETICS 23(3):229-229 FONATSCH C FRAGILE X-CHROMOSOME IN FIBROBLASTS - LONGITUDINAL-STUDY ON TECHNICAL VARIATIONS | 3 | 3 |
| 1007 | 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 |
| 1008 | 5 | 52 | 164 1983 SCHWEIZERISCHE MEDIZINISCHE WOCHENSCHRIFT 113(7):238-244 ZOLLINGER A; SCHMID W; VILAN J; SORG B; KNOBLAUCH M X-LINKED MENTAL-RETARDATION WITH FRAGILE X-CHROMOSOME AND MACROORCHIDISM | 3 | 3 |
| 1009 | 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 |
| 1010 | 0 | 0 | 201 1984 CYTOGENETICS AND CELL GENETICS 37(1-4):587-587 SNYDER FF; LIN CC; HARASYM CA; JAMRO HK; KUSHNIG ML; et al. EVIDENCE FOR CLOSE ASSOCIATION BETWEEN THE FRAGILE X(Q27-28)-CHROMOSOME SITE AND GLUCOSE-6-PHOSPHATE-DEHYDROGENASE (G6PD) BUT NOT WITH HYPOXANTHINE-GUANINE PHOSPHORIBOSYLTRANSFERASE (HPRT) | 3 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1011 | 3 | 7 | 239 1985 ACTA PAEDIATRICA SCANDINAVICA 74(6):974-974 FLOOD A; SANNER G REFRACTIVE ERRORS IN THE FRAGILE-X SYNDROME | 3 | 3 |
| 1012 | 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 |
| 1013 | 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 |
| 1014 | 5 | 24 | 293 1985 JAPANESE JOURNAL OF CANCER RESEARCH 76(10):977-983 HORI T; AYUSAWA D; GLOVER TW; SENO T EXPRESSION OF FRAGILE SITE ON THE HUMAN-X CHROMOSOME IN SOMATIC-CELL HYBRIDS BETWEEN HUMAN FRAGILE-X CELLS AND THYMIDYLATE SYNTHASE-NEGATIVE MOUSE MUTANT-CELLS | 3 | 18 |
| 1015 | 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 |
| 1016 | 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 |
| 1017 | 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 |
| 1018 | 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 |
| 1019 | 4 | 5 | 382 1986 CLINICAL GENETICS 30(4):346-347 SOUDEK D FRAGILE-X - EXPERIENCE OF A LABORATORY | 3 | 3 |
| 1020 | 5 | 12 | 404 1986 LANCET 2(8517):1191-1192 [Anon] PREVENTIVE SCREENING FOR FRAGILE-X SYNDROME | 3 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1021 | 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 |
| 1022 | 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 |
| 1023 | 0 | 0 | 477 1987 JOURNAL OF MEDICAL GENETICS 24(10):635-635 CONNOR JM; OSMAN H; STEPHANIE L; NEVIN NC; HOFKER M LINKAGE ANALYSIS IN FAMILIES WITH THE FRAGILE X SYNDROME USING CX55-7 (DXS105) | 3 | 3 |
| 1024 | 3 | 9 | 520 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):143-147 NIELSEN KB GROWTH-PATTERN IN BOYS WITH FRAGILE-X | 3 | 3 |
| 1025 | 2 | 4 | 526 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 |
| 1026 | 3 | 4 | 557 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 31(4):733-734 WILSON DP; CARPENTER NJ; BERKOVITZ G THYROID-FUNCTION IN MEN WITH FRAGILE X-LINKED MR | 3 | 3 |
| 1027 | 5 | 31 | 571 1988 CANCER 62(11):2383-2386 CUNNINGHAM M; DICKERMAN JD FRAGILE-X SYNDROME AND ACUTE LYMPHOBLASTIC-LEUKEMIA | 3 | 3 |
| 1028 | 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 |
| 1029 | 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 |
| 1030 | 4 | 4 | 657 1989 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 28(6):965-966 FISCH GS FRAGILE-X AND AUTISM | 3 | 4 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1031 | 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 |
| 1032 | 0 | 3 | 669 1989 SCIENCE 243(4888):171-172 BARNES DM FRAGILE-X SYNDROME AND ITS PUZZLING GENETICS | 3 | 9 |
| 1033 | 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 |
| 1034 | 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 |
| 1035 | 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 |
| 1036 | 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 |
| 1037 | 0 | 4 | 815 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):408-410 SHAPIRO LR; WILMOT PL; SHAPIRO DA; PETTERSEN IM; CASAMASSIMA AC CYTOGENETIC DIAGNOSIS OF THE FRAGILE-X SYNDROME - EFFICIENCY, UTILIZATION, AND TRENDS | 3 | 3 |
| 1038 | 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 |
| 1039 | 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 |
| 1040 | 11 | 23 | 900 1991 PRENATAL DIAGNOSIS 11(5):333-338 WEBB T EXPRESSION OF FRAGILE-X IN A FEMALE FETUS DIAGNOSED AFTER CHORIONIC VILLUS SAMPLING | 3 | 4 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1041 | 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 |
| 1042 | 6 | 12 | 933 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):162-166 HOWARDPEEBLES PN; MADDALENA A RECENT EXPERIENCE IN PRENATAL-DIAGNOSIS OF FRAGILE-X | 3 | 3 |
| 1043 | 12 | 25 | 936 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):174-180 VONKOSKULL H; NORDSTROM AM; SALONEN R; PELTONEN L PRENATAL-DIAGNOSIS AND CARRIER DETECTION IN FRAGILE-X | 3 | 3 |
| 1044 | 14 | 40 | 948 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 |
| 1045 | 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 |
| 1046 | 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 |
| 1047 | 38 | 77 | 978 1992 CLINICAL SCIENCE 83(3):255-264 HIRST MC; KNIGHT SJL; BELL MV; SUPER M; DAVIES KE THE FRAGILE-X SYNDROME | 3 | 3 |
| 1048 | 23 | 48 | 982 1992 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 34(9):826-832 GOLDSON E; HAGERMAN RJ THE FRAGILE-X SYNDROME | 3 | 3 |
| 1049 | 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 |
| 1050 | 2 | 2 | 999 1992 JOURNAL OF MEDICAL GENETICS 29(4):287-287 SMART RD FRAGILE X-SYNDROME - AS COMMON AS 1ST THOUGHT | 3 | 4 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1051 | 3 | 10 | 1001 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 |
| 1052 | 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 |
| 1053 | 13 | 25 | 1075 1993 AMERICAN JOURNAL OF MEDICAL GENETICS 45(5):589-593 MILUNSKY A; HUANG XL; AMOS JA; HERSKOWITZ J; FARRER LA; et al. 46,XY/47,XYY MALE WITH THE FRAGILE X-SYNDROME - CYTOGENETIC AND MOLECULAR STUDIES | 3 | 4 |
| 1054 | 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 |
| 1055 | 4 | 14 | 1094 1993 CLINICAL GENETICS 44(2):82-88 LOESCH DZ; SAMPSON ML EFFECT OF THE FRAGILE-X ANOMALY ON BODY PROPORTIONS ESTIMATED BY PEDIGREE ANALYSIS | 3 | 3 |
| 1056 | 7 | 11 | 1095 1993 CLINICAL GENETICS 44(2):109-110 BODURTHA J; JACKSONCOOK C; MADDALENA A; PISERCHIO J; WALLER R 46XY/47XYY MOSAICISM AND FRAGILE-X | 3 | 4 |
| 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 | 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 |
| 1059 | 19 | 24 | 1172 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):281-293 SUTHERLAND GR; BROWN WT; HAGERMAN R; JENKINS E; LUBS H; et al. SIXTH INTERNATIONAL WORKSHOP ON THE FRAGILE-X AND X-LINKED MENTAL-RETARDATION | 3 | 4 |
| 1060 | 8 | 9 | 1176 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):315-316 BUTLER MG; PRATESI R; VNENCAKJONES CL MOLECULAR-GENETIC SCREENING IN CYTOGENETICALLY NORMAL MENTALLY-RETARDED MALES WITH MANIFESTATIONS OF FRAGILE-X-SYNDROME | 3 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1061 | 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 |
| 1062 | 7 | 10 | 1200 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):463-465 RYYNANEN M; PULKKINEN L; KIRKINEN P; SAARIKOSKI S FRAGILE-X SYNDROME IN EAST FINLAND - MOLECULAR APPROACH TO GENETIC AND PRENATAL-DIAGNOSIS | 3 | 4 |
| 1063 | 11 | 13 | 1202 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):471-473 HALLEY D; VANDENOUWELAND A; DEELEN W; VERMA I; OOSTRA B STRATEGY FOR RELIABLE PRENATAL DETECTION OF NORMAL-MALE CARRIERS OF THE FRAGILE-X-SYNDROME | 3 | 4 |
| 1064 | 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 |
| 1065 | 16 | 21 | 1281 1994 PRENATAL DIAGNOSIS 14(6):469-474 STRAIN L; PORTEOUS MEM; GOSDEN CM; ELLIS PM; NEILSON JP; et al. PRENATAL-DIAGNOSIS OF FRAGILE-X-SYNDROME - MANAGEMENT OF THE MALE FETUS WITH A PREMUTATION | 3 | 4 |
| 1066 | 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 |
| 1067 | 2 | 2 | 1491 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):376-376 Burgess B; Partington M; Turner G; Robinson H Normal age of menarche in fragile X syndrome | 3 | 3 |
| 1068 | 20 | 37 | 1506 1996 ARCHIVES DE PEDIATRIE 3(8):814-821 Mornet E; SimonBouy B Molecular biology of fragile X syndrome: Applications to genetic counselling and molecular diagnosis | 3 | 4 |
| 1069 | 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 |
| 1070 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1071 | 35 | 63 | 1571 1996 PRENATAL DIAGNOSIS 16(13):1199-1211 Sutherland GR; Mulley JC Fragile X syndrome and Fragile XE mental retardation | 3 | 9 |
| 1072 | 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 |
| 1073 | 28 | 43 | 1634 1997 ANNALS OF MEDICINE 29(6):563-567 Oostra BA; Hoogeveen AT Animal model for fragile X syndrome | 3 | 8 |
| 1074 | 17 | 20 | 1637 1997 ARCHIVES DE PEDIATRIE 4(3):227-236 Cossee M; Moutou C; Biancalana V; Bouix JC; Plessis G; et al. The fragile X syndrome is still underdiagnosed: Efficacy of molecular testing in mentally retarded probands | 3 | 3 |
| 1075 | 5 | 8 | 1658 1997 HOSPITAL PRACTICE 32(4):73-& Warren ST Trinucleotide repetition and fragile X syndrome | 3 | 5 |
| 1076 | 4 | 60 | 1673 1997 JOURNAL OF BIOLOGICAL CHEMISTRY 272(27):16783-16792 Bacolla A; Gellibolian R; Shimizu M; Amirhaeri S; Kang S; et al. Flexible DNA: Genetically unstable CTG center dot CAG and CGG center dot CCG from human hereditary neuromuscular disease genes | 3 | 57 |
| 1077 | 21 | 32 | 1685 1997 JOURNAL OF MEDICAL GENETICS 34(8):627-631 Kunst CB; Leeflang EP; Iber JC; Arnheim N; Warren ST The effect of FMR1 CGG repeat interruptions on mutation frequency as measured by sperm typing | 3 | 16 |
| 1078 | 12 | 38 | 1686 1997 JOURNAL OF MEDICAL GENETICS 34(11):907-911 vanRijn MA; deVries BBA; Tibben A; vandenOuweland AMW; Halley DJJ; et al. DNA testing for fragile X syndrome: implications for parents and family | 3 | 4 |
| 1079 | 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 |
| 1080 | 7 | 12 | 1730 1998 CLINICAL GENETICS 54(4):366-367 Vatta S; Cigui I; Demori E; Morgutti M; Pecile V; et al. Fragile X syndrome, mental retardation and macroorchidism | 3 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1081 | 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 |
| 1082 | 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 |
| 1083 | 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 |
| 1084 | 14 | 26 | 1758 1998 INDIAN JOURNAL OF MEDICAL RESEARCH 108:12-16 Jain U; Verma IC; Kapoor AK Prevalence of fragile X(A) syndrome in mentally retarded children at a genetics referral centre in Delhi, India | 3 | 4 |
| 1085 | 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 |
| 1086 | 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 |
| 1087 | 7 | 29 | 1782 1998 JOURNAL OF MOLECULAR BIOLOGY 275(1):17-23 Darlow JM; Leach DRF Evidence for two preferred hairpin folding patterns in d(CGG).d(CCG) repeat tracts in vivo | 3 | 21 |
| 1088 | 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 |
| 1089 | 4 | 5 | 1849 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):202-203 Tuncbilek E; Alikasifoglu M; Boduroglu K; Aktas D; Anar B Frequency of fragile X syndrome among Turkish patients with mental retardation of unknown etiology | 3 | 3 |
| 1090 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1091 | 16 | 32 | 1902 1999 HUMAN MUTATION 14(1):71-79 Panagopoulos I; Lassen C; Kristoffersson U; Aman P A methylation PCR approach for detection of fragile X syndrome | 3 | 4 |
| 1092 | 11 | 42 | 1912 1999 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 43:466-474 Garner C; Callias M; Turk J Executive function and theory of mind performance of boys with fragile-X syndrome | 3 | 4 |
| 1093 | 12 | 18 | 1918 1999 JOURNAL OF MEDICAL GENETICS 36(3):253-257 Helderman-van den Enden ATJM; Maaswinkel-Mooij PD; Hoogendoorn E; Willemsen R; Maat-Kievit JA; et al. Monozygotic twin brothers with the fragile X syndrome: different CGG repeats and different mental capacities | 3 | 9 |
| 1094 | 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 |
| 1095 | 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 |
| 1096 | 17 | 20 | 2015 2000 GENETIC TESTING 4(3):289-292 Geva E; Yaron Y; Shomrat R; Ben-Yehuda A; Zabari S; et al. The risk of Fragile X premutation expansion is lower in carriers detected by general prenatal screening than in carriers from known Fragile X families | 3 | 4 |
| 1097 | 35 | 55 | 2023 2000 HUMAN MOLECULAR GENETICS 9(19):2909-2918 Crawford DC; Wilson B; Sherman SL Factors involved in the initial mutation of the fragile X CGG repeat as determined by sperm small pool PCR | 3 | 11 |
| 1098 | 8 | 18 | 2084 2000 NEUROSCIENCE RESEARCH COMMUNICATIONS 26(3):265-277 Bakker CE; Kooy RF; D'Hooge R; Tamanini F; Willemsen R; et al. Introduction of a FMR1 transgene in the fragile X knockout mouse. | 3 | 3 |
| 1099 | 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 |
| 1100 | 0 | 0 | 2096 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):177-177 Hagerman RJ; Greco C; Chudley A; Leehey M; Tassone F; et al. Neuropathology and neurodegenerative features in some older male premutation carriers of fragile X syndrome. | 3 | 4 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1101 | 7 | 18 | 2113 2001 AMERICAN JOURNAL OF MEDICAL GENETICS 100(2):110-115 Stoll C Problems in the diagnosis of fragile X syndrome in young children are still present | 3 | 4 |
| 1102 | 23 | 34 | 2138 2001 CELLULAR AND MOLECULAR NEUROBIOLOGY 21(1):29-38 Castren M; Haapasalo A; Oostra BA; Castren E Subcellular localization of fragile X mental retardation protein with the I304N mutation in the RNA-binding domain in cultured hippocampal neurons | 3 | 3 |
| 1103 | 13 | 31 | 2170 2001 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 22(6):353-359 Myers GF; Mazzocco MMM; Maddalena A; Reiss AL No widespread psychological effect of the fragile X premutation in childhood: Evidence from a preliminary controlled study | 3 | 3 |
| 1104 | 8 | 20 | 2188 2001 NEUROREPORT 12(11):2573-2576 Rojas DC; Benkers TL; Rogers SJ; Teale PD; Reite ML; et al. Auditory evoked magnetic fields in adults with fragile X syndrome | 3 | 4 |
| 1105 | 10 | 37 | 2233 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):923-932 Coffee B; Zhang FP; Ceman S; Warren ST; Reines D Histone modifications depict an aberrantly heterochromatinized FMR1 gene in fragile X syndrome | 3 | 14 |
| 1106 | 27 | 43 | 2238 2002 AMERICAN JOURNAL OF MEDICAL GENETICS 110(3):226-233 Crawford DC; Meadows KL; Newman JL; Taft LF; Scott E; et al. Prevalence of the fragile x syndrome in African-Americans | 3 | 4 |
| 1107 | 11 | 20 | 2257 2002 CURRENT BIOLOGY 12(24):R852-R854 Carthew RW RNA interference: The fragile X syndrome connection | 3 | 10 |
| 1108 | 16 | 35 | 2314 2002 MICROSCOPY RESEARCH AND TECHNIQUE 57(3):168-173 Hagerman RJ; Miller LJ; McGrath-Clarke J; Riley K; Goldson E; et al. Influence of stimulants on electrodermal studies in fragile X syndrome | 3 | 3 |
| 1109 | 19 | 36 | 2334 2002 NUCLEIC ACIDS RESEARCH 30(14):3278-3285 Pietrobono R; Pomponi MG; Tabolacci E; Oostra B; Chiurazzi P; et al. Quantitative analysis of DNA demethylation and transcriptional reactivation of the FMR1 gene in fragile X cells treated with 5-azadeoxycytidine | 3 | 9 |
| 1110 | 18 | 22 | 2340 2002 PRENATAL DIAGNOSIS 22(6):459-462 Rife M; Mallolas J; Badenas C; Tazon B; Miguelez MR; et al. Pilot study for the neonatal screening of fragile X syndrome | 3 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1111 | 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 |
| 1112 | 4 | 6 | 2409 2003 CLINICAL GENETICS 64(1):54-56 Rogers C; Partington MW; Turner GM Tremor, ataxia and dementia in older men may indicate a carrier of the fragile X syndrome | 3 | 4 |
| 1113 | 23 | 44 | 2430 2003 HUMAN MOLECULAR GENETICS 12(23):3067-3074 Chen LS; Tassone F; Sahota P; Hagerman PJ The (CGG)(n) repeat element within the 5 ' untranslated region of the FMR1 message provides both positive and negative cis effects on in vivo translation of a downstream reporter | 3 | 3 |
| 1114 | 18 | 22 | 2447 2003 JOURNAL OF MEDICAL GENETICS 40(5):377-379 Willemsen R; Smits A; Severijnen LA; Jansen M; Jacobs A; et al. Predictive testing for cognitive functioning in female carriers of the fragile X syndrome using hair root analysis | 3 | 3 |
| 1115 | 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 |
| 1116 | 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 |
| 1117 | 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 |
| 1118 | 18 | 58 | 2512 2004 DEVELOPMENTAL BIOLOGY 270(2):290-307 Zhang YQ; Matthies HJG; Mancuso J; Andrews HK; Woodruff E; et al. The Drosophila fragile X-related gene regulates axoneme differentiation during spermatogenesis | 3 | 3 |
| 1119 | 17 | 55 | 2514 2004 EMBO JOURNAL 23(16):3346-3355 Rackham O; Brown CM Visualization of RNA-protein interactions in living cells: FMRP and IMP1 interact on mRNAs | 3 | 4 |
| 1120 | 25 | 53 | 2611 2004 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 101(42):15201-15206 Lu R; Wang HP; Liang Z; Ku L; O'Donnell WT; et al. The fragile X protein controls microtubule-associated protein 1B translation and microtubule stability in brain neuron development | 3 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1121 | 0 | 0 | 5 1980 AMERICAN JOURNAL OF HUMAN GENETICS 32(6):A114-A114 KAISERMCCAW B; HECHT F THE FRAGILE-X - NO DYSMORPHIC SYNDROME, BUT A MARKER | 2 | 2 |
| 1122 | 0 | 0 | 7 1980 ARIZONA MEDICINE 37(11):764-766 HECHT F; KAISERMCCAW B; MOORE BC; CADIEN J; GLOVER TW THE FRAGILE X-CHROMOSOME MENTAL-RETARDATION AND LARGE TESTES | 2 | 2 |
| 1123 | 0 | 1 | 49 1982 AMERICAN JOURNAL OF HUMAN GENETICS 34(6):A149-A149 WANG JC; BOSS GR; MAGNER MT; ERBE RW FOLATE PATHWAYS IN CELLS FROM FRAGILE-X SYNDROME PATIENTS AND CARRIERS | 2 | 3 |
| 1124 | 0 | 0 | 82 1982 NEUROLOGY 32(4):A190-A190 ROSENBERGER PB; WILSONCIAMBRONE S; MILUNSKY A SPEECH FLUENCY DISORDER IN THE FRAGILE-X SYNDROME | 2 | 2 |
| 1125 | 0 | 1 | 95 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A122-A122 WILSON DP; CARPENTER NJ; BERKOVITZ GD; BROWN TR; MIGEON CJ THYROID-FUNCTION IN FRAGILE X-LINKED MENTAL-RETARDATION | 2 | 2 |
| 1126 | 0 | 0 | 96 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A127-A127 BRYANT EM; GLADSTONE P; MARTIN GM EXPRESSION OF THE FRAGILE-X IN MOUSE-X HUMAN SOMATIC-CELL HYBRIDS | 2 | 2 |
| 1127 | 4 | 5 | 109 1983 AMERICAN JOURNAL OF MEDICAL GENETICS 14(4):795-796 DAKER MG FRAGILE X-CHROMOSOME IN NORMAL MALES | 2 | 4 |
| 1128 | 0 | 0 | 122 1983 CLINICAL GENETICS 23(3):232-232 VANDERHAGEN CB; ORSTAVIK KH; BAKKE J; BERG K MONOZYGOUS MALE TRIPLETS WITH MENTAL-RETARDATION AND A FRAGILE X-CHROMOSOME | 2 | 2 |
| 1129 | 0 | 0 | 126 1983 CLINICAL GENETICS 23(3):254-254 VEENEMA H; GERAEDTS JPM THE FRAGILE-X CHROMOSOME SEGREGATING IN A LARGE PEDIGREE | 2 | 2 |
| 1130 | 0 | 0 | 133 1983 CLINICAL RESEARCH 31(2):A290-A290 BRANDA RF; ARTHUR DC; KING RA FRAGILE X PATIENTS HAVE NORMAL FOLATE METABOLISM | 2 | 2 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1131 | 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 |
| 1132 | 3 | 6 | 208 1984 HUMAN GENETICS 68(4):346-347 DEARCE MA VERIFICATION OF LYONS HYPOTHESIS IN FRAGILE-X CARRIERS | 2 | 5 |
| 1133 | 1 | 4 | 224 1984 LANCET 1(8370):220-220 WEBB T; THAKE A; TODD J; BUNDEY S PREVALENCE OF FRAGILE X-CHROMOSOME | 2 | 4 |
| 1134 | 0 | 4 | 226 1984 LANCET 1(8370):220-221 LINNA SL; SIMILA S; HARO E; HERVA R PREVALENCE OF FRAGILE X-CHROMOSOME | 2 | 4 |
| 1135 | 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 |
| 1136 | 7 | 19 | 252 1985 AMERICAN JOURNAL OF MEDICAL GENETICS 22(3):571-575 MITCHELL JA; WRAY J; MICHALSKI K NEUROFIBROMATOSIS AND FRAGILE-X SYNDROME IN THE SAME PATIENT | 2 | 3 |
| 1137 | 0 | 3 | 260 1985 CANADIAN MEDICAL ASSOCIATION JOURNAL 133(5):358-& SOUDEK D FRAGILE-X - A SYMPTOM OF THE DISEASE | 2 | 4 |
| 1138 | 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 |
| 1139 | 0 | 0 | 265 1985 CLINICAL GENETICS 27(3):334-335 SCHMIDT A PRENATAL-DIAGNOSIS OF FRAGILE X-SYNDROME | 2 | 4 |
| 1140 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1141 | 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 |
| 1142 | 1 | 4 | 301 1985 JOURNAL OF MEDICAL GENETICS 22(5):397-397 WINTER RM; PEMBREY ME; DAVIES KE ANALYSIS OF LINKAGE DATA WITH FACTOR-IX CORROBORATES THE HYPOTHESIS THAT A PREMUTATION, FOLLOWED BY A RECOMBINATION EVENT, GENERATES THE FULL MUTATION IN FRAGILE X-LINKED MENTAL-RETARDATION | 2 | 2 |
| 1143 | 4 | 17 | 319 1986 AMERICAN JOURNAL OF HUMAN GENETICS 38(4):533-539 ABRUZZO MA; HUNT PA; MAYER M; JACOBS PA; WANG JCC; et al. A COMPARISON OF FRAGILE X-EXPRESSION IN LYMPHOCYTE AND LYMPHOBLASTOID CULTURES | 2 | 3 |
| 1144 | 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 |
| 1145 | 5 | 16 | 344 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):475-481 JENKINS EC; KASTIN BR; KRAWCZUN MS; LELE KP; SILVERMAN WP; et al. FRAGILE-X CHROMOSOME FREQUENCY IS CONSISTENT TEMPORALLY AND WITHIN REPLICATE CULTURES | 2 | 3 |
| 1146 | 0 | 0 | 396 1986 JOURNAL OF MEDICAL GENETICS 23(2):166-167 CONNOR JM; COLGAN JM; CROSSLEY JA; IMRIE SJ; YATES JRW MULTIPOINT LINKAGE ANALYSIS IN FAMILIES WITH THE FRAGILE-X SYNDROME | 2 | 0 |
| 1147 | 6 | 19 | 405 1986 MUTATION RESEARCH 173(3):201-205 DUNCAN AMV ENHANCED SENSITIVITY OF LYMPHOBLASTOID-CELLS FROM INDIVIDUALS CARRYING THE MUTATION FOR THE FRAGILE X-SYNDROME TO THE CLASTOGENIC EFFECTS OF FUDR | 2 | 3 |
| 1148 | 17 | 31 | 435 1987 BRITISH MEDICAL JOURNAL 295(6598):564-565 KINNELL HG FRAGILE X-SYNDROME - AN IMPORTANT PREVENTABLE CAUSE OF MENTAL HANDICAP | 2 | 2 |
| 1149 | 0 | 15 | 454 1987 HUMAN GENETICS 75(1):4-6 AMAROSE AP; HUTTENLOCHER PR; SPRUDZS RM; LAITSCH TJ; PETTENATI MJ A HERITABLE FRAGILE 12Q24.13 SEGREGATING IN A FAMILY WITH THE FRAGILE X-CHROMOSOME | 2 | 14 |
| 1150 | 10 | 12 | 464 1987 HUMAN GENETICS 77(3):297-298 WINTER R; PEMBREY M INTERPRETATION OF THE HETEROGENEITY IN THE LINKAGE RELATIONSHIPS OF DNA MARKERS AROUND THE FRAGILE-X LOCUS | 2 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1151 | 21 | 49 | 538 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):435-442 KRAWCZUN MS; JENKINS EC; BROWN WT; SILVERMAN WP FRAGILE-X EXPRESSION IN SHORT-TERM WHOLE-BLOOD CULTURES IS AFFECTED BY CELL-DENSITY | 2 | 3 |
| 1152 | 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 |
| 1153 | 8 | 28 | 555 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):697-702 SHABTAI F; HART J; KLAR D; BICHACHO S; HALBRECHT I FRAGILE-X EXPRESSION IN MARTIN-BELL SYNDROME, INTELLECTUALLY NORMAL INDIVIDUALS, AND NEOPLASIA, INTERPRETED BY A VIRAL HYPOTHESIS | 2 | 3 |
| 1154 | 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 |
| 1155 | 7 | 21 | 578 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 |
| 1156 | 20 | 37 | 582 1988 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 30(2):257-261 HO HZ; GLAHN TJ; HO JC THE FRAGILE-X SYNDROME | 2 | 3 |
| 1157 | 3 | 5 | 588 1988 HUMAN GENETICS 78(4):383-383 BUTLER MG; JOSEPH GM; RAMES LJ; CACHEIRO N; LOZZIO CB CHROMOSOME BREAKAGE IN CONTROL AND FRAGILE-X SUBJECTS USING FOLATE-DEFICIENT CULTURE CONDITIONS | 2 | 2 |
| 1158 | 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 |
| 1159 | 1 | 11 | 603 1988 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 18(4):681-685 TSAI LY; CROWE RR; PATIL SR; MURRAY J; QUINN J SEARCH FOR DNA MARKERS IN 2 AUTISTIC MALES WITH THE FRAGILE-X SYNDROME | 2 | 3 |
| 1160 | 4 | 10 | 618 1989 AMERICAN JOURNAL OF HUMAN GENETICS 45(6):977-978 FERRI R BRAIN-STEM AUDITORY EVOKED-POTENTIALS IN THE FRAGILE-X SYNDROME | 2 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1161 | 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 |
| 1162 | 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 |
| 1163 | 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 |
| 1164 | 10 | 17 | 647 1989 HUMAN GENETICS 82(1):79-81 SCHAAP T THE ROLE OF RECOMBINATION IN THE EVOLVEMENT OF THE FRAGILE X-MUTATION | 2 | 2 |
| 1165 | 3 | 4 | 658 1989 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 28(6):966-966 PAYTON JB; STEELE MW; WENGER SL; MINSHEW NJ FRAGILE-X AND AUTISM | 2 | 2 |
| 1166 | 0 | 0 | 660 1989 M S-MEDECINE SCIENCES 5(7):450-458 JORDAN BR; MATTEI JF FRAGILE X-LINKED MENTAL-RETARDATION, 1989 | 2 | 2 |
| 1167 | 2 | 4 | 695 1990 ARCHIVES OF DISEASE IN CHILDHOOD 65(3):335-335 REDINGTON A; BUSH A FRAGILE-X MENTAL-RETARDATION | 2 | 2 |
| 1168 | 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 |
| 1169 | 0 | 1 | 726 1990 LANCET 336(8723):1131-1131 TEMPLE IK; BARAITSER M; PEMBREY ME; BUTLER L; JACOBS P; et al. UNUSUAL PRESENTATION OF FRAGILE-X SYNDROME | 2 | 3 |
| 1170 | 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 |
| 1171 | 16 | 47 | 796 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):298-304 GLASS IA; PIRRIT LA; WHITE EM; BELL MV; DAVIES KE; et al. LINKAGE ANALYSIS IN THE FRAGILE-X SYNDROME USING MULTIPLE DISTAL XQ POLYMORPHIC DNA MARKERS | 2 | 2 |
| 1172 | 2 | 9 | 797 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):305-310 MURPHY PD; WATSON MS; SHAPIRO LR; WILMOT PL; BREG WR DNA-BASED GENETIC TESTING IN 50 FRAGILE-X FAMILIES | 2 | 2 |
| 1173 | 16 | 20 | 804 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):349-353 CARPENTER NJ; THIBODEAU SN; BROWN WT LINKAGE RELATIONSHIPS BETWEEN DXS105, DXS98, AND OTHER POLYMORPHIC DNA MARKERS FLANKING THE FRAGILE-X LOCUS | 2 | 3 |
| 1174 | 7 | 11 | 805 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):363-366 DRUGGE U; BLOMQUIST HK; GUSTAVSON KH; HOLMGREN G FRAGILE-X FAMILIES IN A NORTHERN SWEDISH COUNTY - A GENEALOGICAL STUDY OF POSSIBLY AFFECTED INDIVIDUALS IN THE 19TH-CENTURY | 2 | 2 |
| 1175 | 13 | 25 | 808 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):374-377 VOELCKEL MA; PELLISSIER MC; PIQUET C; NGUYEN C; BOCCACCIO I; et al. FRAGILE-X SYNDROME IN AN EXTENDED FAMILY WITH SPECIAL REFERENCE TO AN AFFECTED MALE WITH KLINEFELTER SYNDROME | 2 | 2 |
| 1176 | 4 | 7 | 812 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):396-399 SHERMAN SL COLLABORATIVE PROSPECTIVE-STUDY OF THE FRAGILE-X SYNDROME - REQUEST FOR PARTICIPATION | 2 | 2 |
| 1177 | 2 | 4 | 821 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):445-446 HOWARDPEEBLES PN FRAGILE-X EXPRESSION - USE OF A DOUBLE INDUCTION SYSTEM | 2 | 4 |
| 1178 | 0 | 0 | 851 1991 CLINICAL RESEARCH 39(1):A1-A1 GOLDSON E; HAGERMAN RJ TEMPERAMENT AND THE FRAGILE-X SYNDROME | 2 | 2 |
| 1179 | 9 | 28 | 853 1991 COMPREHENSIVE PSYCHIATRY 32(1):83-87 TRANEBAERG L; ORUM A MAJOR DEPRESSIVE DISORDER AS A PROMINENT BUT UNDERESTIMATED FEATURE OF FRAGILE-X SYNDROME | 2 | 4 |
| 1180 | 2 | 8 | 867 1991 HUMAN GENETICS 87(1):95-96 KAHKONEN M; HAATAJA R; LEISTI J URIDINE ENHANCES EXPRESSION OF THE FRAGILE-X CHROMOSOME IN HUMAN-LYMPHOCYTES | 2 | 2 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1181 | 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 |
| 1182 | 7 | 11 | 891 1991 NATURE 351(6326):439-440 DAVIES K HUMAN-GENETICS - BREAKING THE FRAGILE-X | 2 | 7 |
| 1183 | 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 |
| 1184 | 0 | 0 | 904 1991 SCIENCE 252(5009):1070-1070 HOFFMAN M UNRAVELING THE GENETICS OF FRAGILE X-SYNDROME | 2 | 4 |
| 1185 | 2 | 9 | 919 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):61-64 REISS AL; CIANCHETTI C; COHEN IL; DEVRIES B; HAGERMAN R; et al. BRIEF SCREENING QUESTIONNAIRE FOR DETERMINING AFFECTED STATE IN FRAGILE-X SYNDROME - A CONSENSUS RECOMMENDATION | 2 | 3 |
| 1186 | 6 | 10 | 927 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):120-123 PARTINGTON MW; ROBINSON H; LAING S; TURNER G MORTALITY IN THE FRAGILE-X SYNDROME - PRELIMINARY DATA | 2 | 3 |
| 1187 | 11 | 26 | 950 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):307-311 VAISANEN ML; KAHKONEN M; LEISTI J CARRIER DETECTION OF THE FRAGILE-X SYNDROME WITH FLANKING RFLP MARKERS AND LINKAGE ANALYSIS | 2 | 2 |
| 1188 | 15 | 21 | 952 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 |
| 1189 | 6 | 8 | 957 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):355-360 SHERMAN SL; BARBI G; BRONDUMNIELSEN K; BROWN WT; CARPENTER NJ; et al. COLLABORATIVE PROSPECTIVE-STUDY OF THE FRAGILE-X SYNDROME - ONE-YEAR PROGRESS REPORT | 2 | 4 |
| 1190 | 7 | 15 | 961 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(6):1057-1062 WEBB T DELAYED REPLICATION OF XQ27 IN INDIVIDUALS WITH THE FRAGILE X-SYNDROME | 2 | 16 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1191 | 37 | 55 | 989 1992 HUMAN GENETICS 88(3):335-343 FOLLETTE PJ; LAIRD CD ESTIMATING THE STABILITY OF THE PROPOSED IMPRINTED STATE OF THE FRAGILE-X MUTATION WHEN TRANSMITTED BY FEMALES | 2 | 3 |
| 1192 | 1 | 11 | 1077 1993 AMERICAN JOURNAL OF MEDICAL GENETICS 46(6):685-686 MIGEON BR ROLE OF DNA METHYLATION IN X-INACTIVATION AND THE FRAGILE X-SYNDROME | 2 | 3 |
| 1193 | 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 |
| 1194 | 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 |
| 1195 | 9 | 24 | 1147 1993 MENTAL RETARDATION 31(4):221-227 WILSON PG; MAZZOCCO MMM AWARENESS AND KNOWLEDGE OF FRAGILE-X SYNDROME AMONG SPECIAL EDUCATORS | 2 | 3 |
| 1196 | 18 | 21 | 1148 1993 MENTAL RETARDATION 31(5):279-283 SMITH SE COGNITIVE DEFICITS ASSOCIATED WITH FRAGILE-X SYNDROME | 2 | 3 |
| 1197 | 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 |
| 1198 | 7 | 18 | 1247 1994 INTELLIGENCE 19(1):45-50 DANIELS JK; OWEN MJ; MCGUFFIN P; THOMPSON L; DETTERMAN DK; et al. IQ AND VARIATION IN THE NUMBER OF FRAGILE-X CGG REPEATS - NO ASSOCIATION IN A NORMAL SAMPLE | 2 | 9 |
| 1199 | 13 | 16 | 1252 1994 JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION 271(7):552-553 CASKEY CT FRAGILE-X SYNDROME - IMPROVING UNDERSTANDING AND DIAGNOSIS | 2 | 2 |
| 1200 | 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 |