UNKNOWN SYNDROME - HOLOPROSENCEPHALY, CONGENITAL HEART-DEFECTS, AND POLYDACTYLY

被引:32
作者
YOUNG, ID [1 ]
MADDERS, DJ [1 ]
机构
[1] LEICESTER ROYAL INFIRM,DEPT HISTOPATHOL,LEICESTER LE2 7LX,ENGLAND
关键词
D O I
10.1136/jmg.24.11.714
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:714 / 715
页数:2
相关论文
共 3 条
[1]   SPECTRUM OF ANOMALIES IN THE MECKEL SYNDROME, OR - MAYBE THERE IS A MALFORMATION SYNDROME WITH AT LEAST ONE CONSTANT ANOMALY [J].
FRASER, FC ;
LYTWYN, A .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1981, 9 (01) :67-73
[2]  
SALONEN R, 1981, CLIN GENET, V19, P321
[3]   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