THE EARLY RECOGNITION OF THE 21-HYDROXYLASE DEFICIENCY VARIETY OF CONGENITAL ADRENAL-HYPERPLASIA

被引：23

作者：

STEEN, G

TAS, AC

TENNOEVERDEBRAUW, MC

DRAYER, NM

WOLTHERS, BG

机构：

[1] STATE UNIV GRONINGEN HOSP,CENT LAB CLIN CHEM,GRONINGEN,NETHERLANDS

[2] STATE UNIV GRONINGEN HOSP,DEPT PEDIAT,DIV ENDOCRINOL,GRONINGEN,NETHERLANDS

[3] CIVO TNO,CENT INST NUTR & FOOD RES,ZEIST,NETHERLANDS

来源：

CLINICA CHIMICA ACTA | 1980年 / 105卷 / 02期

关键词：

D O I：

10.1016/0009-8981(80)90463-5

中图分类号：

R446 [实验室诊断]; R-33 [实验医学、医学实验];

学科分类号：

1001 ;

摘要：

引用

页码：213 / 224

页数：12

共 24 条

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[7] VARIATIONS IN URINARY STEROID PROFILES AFTER BIRTH [J].

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HORNING, EC .

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[8]

HUGHES IA, 1977, CAN MED ASSOC J, V117, P363

[9] APPLICATION OF A SERUM 170H-PROGESTERONE RADIOIMMUNOASSAY TO DIAGNOSIS AND MANAGEMENT OF CONGENITAL ADRENAL-HYPERPLASIA [J].

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[10]

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