LINKAGE ANALYSIS OF THE RETT SYNDROME USING HUMAN CHROMOSOMAL SPECIFIC PROBES

被引:14
作者
ANVRET, M
JOHANSSON, IM
WAHLSTROM, J
HAGBERG, B
机构
[1] GOTHENBURG UNIV, E HOSP, DEPT PEDIAT 2, S-41685 GOTHENBURG, SWEDEN
[2] GOTHENBURG UNIV, E HOSP, DEPT MED BIOCHEM, S-41685 GOTHENBURG, SWEDEN
[3] OSTRA SJUKHUSET, DEPT CLIN GENET, S-41685 GOTHENBURG, SWEDEN
关键词
D O I
10.1016/S0387-7604(85)80045-0
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
引用
收藏
页码:361 / 364
页数:4
相关论文
共 17 条
  • [1] THE GENE STRUCTURE OF HUMAN ANTI-HEMOPHILIC FACTOR-IX
    ANSON, DS
    CHOO, KH
    REES, DJG
    GIANNELLI, F
    GOULD, K
    HUDDLESTON, JA
    BROWNLEE, GG
    [J]. EMBO JOURNAL, 1984, 3 (05) : 1053 - 1060
  • [2] EVIDENCE FOR INTEGRATED EBV GENOMES IN RAJI CELLULAR DNA
    ANVRET, M
    KARLSSON, A
    BJURSELL, G
    [J]. NUCLEIC ACIDS RESEARCH, 1984, 12 (02) : 1149 - 1161
  • [3] CLOSE GENETIC-LINKAGE BETWEEN X-LINKED RETINITIS PIGMENTOSA AND A RESTRICTION FRAGMENT LENGTH POLYMORPHISM IDENTIFIED BY RECOMBINANT DNA PROBE L1.28
    BHATTACHARYA, SS
    WRIGHT, AF
    CLAYTON, JF
    PRICE, WH
    PHILLIPS, CI
    MCKEOWN, CME
    JAY, M
    BIRD, AC
    PEARSON, PL
    SOUTHERN, EM
    EVANS, HJ
    [J]. NATURE, 1984, 309 (5965) : 253 - 255
  • [4] BOTSTEIN D, 1980, AM J HUM GENET, V32, P314
  • [5] LINKAGE ANALYSIS OF 2 CLONED DNA-SEQUENCES FLANKING THE DUCHENNE MUSCULAR-DYSTROPHY LOCUS ON THE SHORT ARM OF THE HUMAN X-CHROMOSOME
    DAVIES, KE
    PEARSON, PL
    HARPER, PS
    MURRAY, JM
    OBRIEN, T
    SARFARAZI, M
    WILLIAMSON, R
    [J]. NUCLEIC ACIDS RESEARCH, 1983, 11 (08) : 2303 - 2312
  • [6] GENETIC-MAPPING OF THE HUMAN X-CHROMOSOME BY USING RESTRICTION FRAGMENT LENGTH POLYMORPHISMS
    DRAYNA, D
    DAVIES, K
    HARTLEY, D
    MANDEL, JL
    CAMERINO, G
    WILLIAMSON, R
    WHITE, R
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (09): : 2836 - 2839
  • [7] A PROGRESSIVE SYNDROME OF AUTISM, DEMENTIA, ATAXIA, AND LOSS OF PURPOSEFUL HAND USE IN GIRLS - RETTS SYNDROME - REPORT OF 35 CASES
    HAGBERG, B
    AICARDI, J
    DIAS, K
    RAMOS, O
    [J]. ANNALS OF NEUROLOGY, 1983, 14 (04) : 471 - 479
  • [8] RETTS SYNDROME - PREVALENCE AND IMPACT ON PROGRESSIVE SEVERE MENTAL-RETARDATION IN GIRLS
    HAGBERG, B
    [J]. ACTA PAEDIATRICA SCANDINAVICA, 1985, 74 (03): : 405 - 408
  • [9] THE MENDELIAN INHERITANCE OF A HUMAN X-CHROMOSOME-SPECIFIC DNA-SEQUENCE POLYMORPHISM AND ITS USE IN LINKAGE STUDIES OF GENETIC-DISEASE
    HILL, MEE
    DAVIES, KE
    HARPER, P
    WILLIAMSON, R
    [J]. HUMAN GENETICS, 1982, 60 (03) : 222 - 226
  • [10] LITTLE PFR, 1981, GENETIC ENG, V1, P61