DETECTION OF THE HETEROZYGOUS STATE IN SIBLINGS OF PATIENTS WITH CONGENITAL ADRENAL-HYPERPLASIA DUE TO 21-HYDROXYLASE DEFICIENCY

被引：20
|
作者：
GUTAI, JP
LEE, PA
JOHNSONBAUGH, RE
GAREIS, F
URBAN, MD
MIGEON, CJ
机构：
[1] JOHNS HOPKINS UNIV HOSP, DEPT PEDIAT, PEDIAT ENDOCRINE CLIN, BALTIMORE, MD 21205 USA
[2] JOHNS HOPKINS UNIV, SCH MED, BALTIMORE, MD 21218 USA
[3] NATL NAVAL MED CTR, DEPT PEDIAT, DIV ENDOCRINE, BETHESDA, MD 20014 USA
[4] USN, REG MED CTR, DEPT PEDIAT, SAN DIEGO, CA 92134 USA
[5] UNIFORMED SERV UNIV HLTH SCI, BETHESDA, MD USA
来源：
JOURNAL OF PEDIATRICS | 1979年 / 94卷 / 05期
关键词：
D O I：
10.1016/S0022-3476(79)80152-3
中图分类号：
R72 [儿科学];
学科分类号：
100202 ;
摘要：
引用
收藏
页码：770 / 772
页数：3
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