Novel Mutation in Two Related 46, XY Phenotypic Females with 17β-Hydroxysteroid Dehydrogenase 3 Deficiency

被引：0
|
作者：
German, Alina [1 ,2 ,3 ]
Tiosano, Dov [3 ,4 ]
Chertin, Boris [5 ]
Nadeem, Sabea [6 ]
Tenenbaum-Rakover, Yardena [7 ,8 ]
机构：
[1] Bnai Zion Med Ctr, Pediat Dept, Haifa, Israel
[2] Clalit Hlth Serv, Haifa, Israel
[3] Meyer Childrens Hosp, Pediat Endocrine Unit, Haifa, Israel
[4] Technion, Rappaport Fac Med, Haifa, Israel
[5] Shaare Zedek Med Ctr, Pediat Urol, Jerusalem, Israel
[6] Clalit Hlth Serv, Haifa, Northern Region, Israel
[7] HaEmek Med Ctr, Pediat Endocrine Inst, Afula, Israel
[8] Rappaport Fac Med, Haifa, Israel
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-P323
引用
收藏
页码：577 / 577
页数：1
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