A Turkish Family with 46,XY Disorder of Sex Development Due to 17b-Hydroxysteroid Dehydrogenase Type 3 Deficiency

被引：0
|
作者：
Gurbuz, Fatih [1 ]
Turan, Ihsan [1 ]
Tastan, Mehmet [1 ]
Yuksel, Bilgin [1 ]
机构：
[1] Cukurova Univ, Pediat Endocrinol, Adana, Turkey
来源：
HORMONE RESEARCH IN PAEDIATRICS | 2018年 / 90卷
关键词：
D O I：
暂无
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
P3-P336
引用
收藏
页码：582 / 582
页数：1
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