PRENATAL-DIAGNOSIS OF X-LINKED CHOROIDEREMIA WITH MENTAL-RETARDATION, ASSOCIATED WITH A CYTOLOGICALLY DETECTABLE X-CHROMOSOME DELETION

被引:54
作者
HODGSON, SV
ROBERTSON, ME
FEAR, CN
GOODSHIP, J
MALCOLM, S
JAY, B
BOBROW, M
PEMBREY, ME
机构
[1] UNITED MED & DENT SCH GUYS & ST THOMAS HOSP,PAEDIAT RES UNIT,GUYS TOWER,LONDON BRIDGE,LONDON SE1 9RT,ENGLAND
[2] MOORFIELDS EYE HOSP,INST OPHTHALMOL,LONDON E1,ENGLAND
[3] INST CHILD HLTH,MOTHERCARE UNIT PAEDIAT GENET,LONDON WC1N 1EH,ENGLAND
关键词
D O I
10.1007/BF00281076
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:286 / 290
页数:5
相关论文
共 23 条
  • [1] BELL A G, 1971, Clinical Genetics, V2, P239
  • [2] FERGUSONSMITH MA, 1982, CYTOGENET CELL GENET, V32, P273
  • [3] FRANCKE U, 1984, CYTOGENET CELL GENET, V38, P298, DOI 10.1159/000132078
  • [4] CHOROIDEREMIA-LOCUS MAPS BETWEEN DXS3 AND DXS11 ON XQ
    GAL, A
    BRUNSMANN, F
    HOGENKAMP, D
    RUTHER, K
    AHLERT, D
    WIENKER, TF
    HAMMERSTEIN, W
    PAWLOWITZKI, IH
    [J]. HUMAN GENETICS, 1986, 73 (02) : 123 - 126
  • [5] DIFFERENT PATTERNS OF X-CHROMOSOME INACTIVITY IN LYMPHOCYTES AND FIBROBLASTS OF A HUMAN BALANCED-X - AUTOSOME TRANSLOCATION
    HELLKUHL, B
    DELACHAPELLE, A
    GRZESCHIK, KH
    [J]. HUMAN GENETICS, 1982, 60 (02) : 126 - 129
  • [6] LEUKOCYTES CULTURED FROM SMALL INOCULA OF WHOLE BLOOD AND PREPARATION OF METAPHASE CHROMOSOMES BY TREATMENT WITH HYPOTONIC KCL
    HUNGERFORD, DA
    [J]. STAIN TECHNOLOGY, 1965, 40 (06): : 333 - +
  • [7] KAOSAAR M, 1980, HUM GENET, V53, P275
  • [8] MAPPING OF THE X-LINKED AGAMMAGLOBULINEMIA LOCUS BY USE OF RESTRICTION-FRAGMENT-LENGTH-POLYMORPHISM
    KWAN, SP
    KUNKEL, L
    BRUNS, G
    WEDGWOOD, RJ
    LATT, S
    ROSEN, FS
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1986, 77 (02) : 649 - 652
  • [9] MICROFLUOROMETRIC DETECTION OF DEOXYRIBONUCLEIC-ACID REPLICATION IN HUMAN METAPHASE CHROMOSOMES
    LATT, SA
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1973, 70 (12) : 3395 - 3399
  • [10] GENE LOCALIZATION OF X-LINKED HYPOHIDROTIC ECTODERMAL DYSPLASIA (C-S-T SYNDROME)
    MACDERMOT, KD
    WINTER, RM
    MALCOLM, S
    [J]. HUMAN GENETICS, 1986, 74 (02) : 172 - 173