UNUSUAL HETEROZYGOTES (HE) OF CONGENITAL ADRENAL-HYPERPLASIA (CAH) DUE TO 21-HYDROXYLASE DEFICIENCY

被引：0

作者：

ZACHMANN, M ^{[1
]}

PRADER, A ^{[1
]}

机构：

[1] UNIV ZURICH,DEPT PAEDIAT,CH-8006 ZURICH,SWITZERLAND

来源：

PEDIATRIC RESEARCH | 1978年 / 12卷 / 02期

关键词：

D O I：

10.1203/00006450-197802000-00107

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

引用

页码：164 / 164

页数：1

共 50 条

[1] UNUSUAL HETEROZYGOTES OF CONGENITAL ADRENAL-HYPERPLASIA DUE TO 21-HYDROXYLASE DEFICIENCY
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[J]. ACTA ENDOCRINOLOGICA, 1978, 87 (03): : 557 - 565
[2] SELECTIVE SCREENING FOR CONGENITAL ADRENAL-HYPERPLASIA (CAH) DUE TO 21-HYDROXYLASE DEFICIENCY
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[J]. ACTA ENDOCRINOLOGICA, 1979, 92 (03): : 542 - 546
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[J]. ACTA ENDOCRINOLOGICA, 1987, 114 : 173 - 174
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[J]. GEBURTSHILFE UND FRAUENHEILKUNDE, 1992, 52 (10) : 586 - 588
[8] 21-HYDROXYLASE DEFICIENCY CONGENITAL ADRENAL-HYPERPLASIA
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[J]. JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1994, 48 (01): : 15 - 22
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[10] PRENATAL DIAGNOSIS OF CONGENITAL ADRENAL-HYPERPLASIA DUE TO 21-HYDROXYLASE DEFICIENCY
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