NEONATAL SCREENING FOR CONGENITAL ADRENAL-HYPERPLASIA

被引：40

作者：

CACCIARI, E ^{[1
]}

BALSAMO, A ^{[1
]}

CASSIO, A ^{[1
]}

PIAZZI, S ^{[1
]}

BERNARDI, F ^{[1
]}

SALARDI, S ^{[1
]}

CICOGNANI, A ^{[1
]}

PIRAZZOLI, P ^{[1
]}

ZAPPULLA, F ^{[1
]}

CAPELLI, M ^{[1
]}

PAOLINI, M ^{[1
]}

机构：

[1] S ORSOLA HOSP,CENT LAB,BOLOGNA,ITALY

来源：

ARCHIVES OF DISEASE IN CHILDHOOD | 1983年 / 58卷 / 10期

关键词：

D O I：

10.1136/adc.58.10.803

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

引用

页码：803 / 806

页数：4

共 16 条

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[9] ACQUIRED ADRENAL-HYPERPLASIA WITH 21-HYDROXYLASE DEFICIENCY IS NOT THE SAME GENETIC DISORDER AS CONGENITAL ADRENAL-HYPERPLASIA [J].

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[10] MICROFILTER PAPER METHOD FOR 17 ALPHA-HYDROXYPROGESTERONE RADIOIMMUNOASSAY - ITS APPLICATION FOR RAPID SCREENING FOR CONGENITAL ADRENAL-HYPERPLASIA [J].

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