UNKNOWN SYNDROME - HIRSCHSPRUNGS-DISEASE, MICROCEPHALY, AND IRIS COLOBOMA - A NEW SYNDROME OF DEFECTIVE NEURONAL MIGRATION

被引:53
作者
HURST, JA
MARKIEWICZ, M
KUMAR, D
BRETT, EM
机构
[1] HOSP SICK CHILDREN,DEPT CLIN GENET,LONDON WC1N 3JH,ENGLAND
[2] HOSP SICK CHILDREN,DEPT NEUROL,LONDON WC1N 3JH,ENGLAND
[3] CTR HUMAN GENET,SHEFFIELD S10 5DN,ENGLAND
关键词
D O I
10.1136/jmg.25.7.494
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:494 / 497
页数:4
相关论文
共 5 条
[1]  
FARNDON PA, 1983, ARCH DIS CHILD, V58, P932, DOI 10.1136/adc.58.11.932
[2]   BILATERAL BICOLORED IRIDES WITH HIRSCHSPRUNGS-DISEASE - A NEURAL CREST SYNDROME [J].
LIANG, JC ;
JUAREZ, CP ;
GOLDBERG, MF .
ARCHIVES OF OPHTHALMOLOGY, 1983, 101 (01) :69-73
[3]   ASSOCIATION OF WAARDENBURG SYNDROME AND HIRSCHSPRUNG MEGACOLON [J].
OMENN, GS ;
MCKUSICK, VA .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1979, 3 (03) :217-223
[4]   WHITE FORELOCK, PIGMENTARY DISORDER OF IRIDES, AND LONG SEGMENT HIRSCHSPRUNG DISEASE - POSSIBLE VARIANT OF WAARDENBURG SYNDROME [J].
SHAH, KN ;
DALAL, SJ ;
DESAI, MP ;
SHETH, PN ;
JOSHI, NC ;
AMBANI, LM .
JOURNAL OF PEDIATRICS, 1981, 99 (03) :432-435
[5]   A COMPUTERIZED DATA-BASE FOR THE DIAGNOSIS OF RARE DYSMORPHIC SYNDROMES [J].
WINTER, RM ;
BARAITSER, M ;
DOUGLAS, JM .
JOURNAL OF MEDICAL GENETICS, 1984, 21 (02) :121-123