21-Hydroxylase Deficiency: Newborn Screening in Iran?

被引：0
|
作者：
Mahdieh, Nejat [2 ,3 ]
Rabbani, Bahareh [2 ]
Rabbani, Ali [1 ,2 ]
机构：
[1] Univ Tehran Med Sci, Pediat Ctr Excellence, Childrens Med Ctr Hosp, Tehran, Iran
[2] Univ Tehran Med Sci, Growth & Dev Res Ctr, Tehran, Iran
[3] Ilam Univ Med Sci, Fac Med, Ilam, Iran
来源：
IRANIAN JOURNAL OF PEDIATRICS | 2012年 / 22卷 / 03期
关键词：
21-hydroxylase Deficiency; Congenital Adrenal Hyperplasia; Screening; CONGENITAL ADRENAL-HYPERPLASIA; CYP21A2; GENE; DIAGNOSIS;
D O I：
暂无
中图分类号：
R72 [儿科学];
学科分类号：
100202 ;
摘要：
引用
收藏
页码：279 / 280
页数：2
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