SISTER CHROMATID EXCHANGE ANALYSIS IN THE PRADER-LABHART-WILLI SYNDROME

被引:8
作者
BUTLER, MG
JENKINS, BB
机构
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1987年 / 28卷 / 04期
关键词
D O I
10.1002/ajmg.1320280406
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:821 / 827
页数:7
相关论文
共 6 条
  • [1] CLINICAL AND CYTOGENETIC SURVEY OF 39 INDIVIDUALS WITH PRADER-LABHART-WILLI SYNDROME
    BUTLER, MG
    MEANEY, FJ
    PALMER, CG
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1986, 23 (03): : 793 - 809
  • [2] HUMMEL M, 1986, American Journal of Human Genetics, V39, pA117
  • [3] LEDBETTER DH, 1982, AM J HUM GENET, V34, P278
  • [4] CHROMOSOME-15 ANOMALIES AND THE PRADER-WILLI SYNDROME - CYTOGENETIC ANALYSIS
    MATTEI, MG
    SOUIAH, N
    MATTEI, JF
    [J]. HUMAN GENETICS, 1984, 66 (04) : 313 - 334
  • [5] NEW GIEMSA METHOD FOR DIFFERENTIAL STAINING OF SISTER CHROMATIDS
    PERRY, P
    WOLFF, S
    [J]. NATURE, 1974, 251 (5471) : 156 - 158
  • [6] WATANABE T, 1984, SISTER CHROMATID EXC, P939