HEREDITARY APLASIA CUTIS CONGENITA AND ASSOCIATED DEFECTS - 3 INSTANCES IN ONE FAMILY AND A SURVEY OF REPORTED CASES

被引:38
作者
MCMURRAY, BR
MARTIN, LW
STJOHNDIGNAN, P
FOGELSON, MH
机构
[1] UNIV CINCINNATI,CHILDRENS HOSP,MED CTR,COLL MED,CINCINNATI,OH 45229
[2] UNIV AFFILIATED CINCINNATI CTR DEV DISORDERS,CINCINNATI,OH 45229
关键词
D O I
10.1177/000992287701600705
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
引用
收藏
页码:610 / 614
页数:5
相关论文
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