INV DUP(15) SUPERNUMERARY MARKER CHROMOSOMES

被引:80
作者
WEBB, T
机构
[1] Department of Clinical Genetics, Birmingham Maternity Hospital, Edgbaston
关键词
D O I
10.1136/jmg.31.8.585
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
[No abstract available]
引用
收藏
页码:585 / 594
页数:10
相关论文
共 56 条
  • [1] 44 PROBANDS WITH AN ADDITIONAL MARKER CHROMOSOME
    BUCKTON, KE
    SPOWART, G
    NEWTON, MS
    EVANS, HJ
    [J]. HUMAN GENETICS, 1985, 69 (04) : 353 - 370
  • [2] MOLECULAR CYTOGENETIC AND CLINICAL-STUDIES OF 42 PATIENTS WITH MARKER CHROMOSOMES
    CALLEN, DF
    EYRE, H
    YIP, MY
    FREEMANTLE, J
    HAAN, EA
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1992, 43 (04): : 709 - 715
  • [3] PARENTAL ORIGIN OF DENOVO CHROMOSOME REARRANGEMENTS
    CHAMBERLIN, J
    MAGENIS, RE
    [J]. HUMAN GENETICS, 1980, 53 (03) : 343 - 347
  • [4] DEFALCO JE, 1978, AM J HUM GENET, V30, pA77
  • [5] FREIDRICH V, 1974, CLIN GENET, V6, P23
  • [6] AN EXTRA IDIC(15P)(Q11) CHROMOSOME IN PRADER-WILLI SYNDROME
    FUJITA, H
    SAKAMOTO, Y
    HAMAMOTO, Y
    [J]. HUMAN GENETICS, 1980, 55 (03) : 409 - 411
  • [7] GENTILE M, 1993, CLIN GENET, V44, P71
  • [8] INV DUP (15) WITH MENTAL-RETARDATION BUT FEW DYSMORPHIC FEATURES
    GILMORE, DH
    BOYD, E
    MCCLURE, JP
    BATSTONE, P
    CONNOR, JM
    [J]. JOURNAL OF MEDICAL GENETICS, 1984, 21 (03) : 221 - 223
  • [9] GOH K, 1984, CLIN GENET, V26, P597
  • [10] HOO JJ, 1986, CLIN GENET, V29, P241