WHITE FORELOCK, PIGMENTARY DISORDER OF IRIDES, AND LONG SEGMENT HIRSCHSPRUNG DISEASE - POSSIBLE VARIANT OF WAARDENBURG SYNDROME

被引:128
作者
SHAH, KN [1 ]
DALAL, SJ [1 ]
DESAI, MP [1 ]
SHETH, PN [1 ]
JOSHI, NC [1 ]
AMBANI, LM [1 ]
机构
[1] BAI JERBAI WADIA HOSP CHILDREN, INST REPROD RES, BOMBAY 400012, MAHARASHTRA, INDIA
关键词
D O I
10.1016/S0022-3476(81)80339-3
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
引用
收藏
页码:432 / 435
页数:4
相关论文
共 11 条
  • [1] STUDIES ON MEGACOLON IN PIEBALD MICE
    BIELSCHOWSKY, M
    SCHOFIELD, GC
    [J]. AUSTRALIAN JOURNAL OF EXPERIMENTAL BIOLOGY AND MEDICAL SCIENCE, 1962, 43 (05): : 395 - +
  • [2] WAARDENBURGS SYNDROME
    DIGEORGE, AM
    OLMSTED, RW
    HARLEY, RD
    [J]. JOURNAL OF PEDIATRICS, 1960, 57 (05) : 649 - 669
  • [3] HAGEMAN MJ, 1977, AM J HUM GENET, V29, P468
  • [4] MCKUSICK VA, 1973, NEW ENGL J MED, V288, P691
  • [5] MCKUSICK VA, 1975, MENDELIAN INHERITANC, P490
  • [6] NIZUKOSHI O, 1958, OTOLARYNGOLOGY-TOKYO, V7, P261
  • [7] ASSOCIATION OF WAARDENBURG SYNDROME AND HIRSCHSPRUNG MEGACOLON
    OMENN, GS
    MCKUSICK, VA
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1979, 3 (03): : 217 - 223
  • [8] SMITH DW, 1976, RECOGNIZABLE PATTERN, P124
  • [9] TELFER MA, 1971, AM J HUM GENET, V23, P383
  • [10] WAARDENBURG PJ, 1951, AM J HUM GENET, V3, P195