Identification of a novel SRY-mutation causing 46,XY complete gonadal dysgenesis in two half-sisters by paternal gonadal mosaicism

被引：0
|
作者：
Filges, Isabel [2 ]
Boesch, Nemya [2 ]
Tschudin, Sibil [3 ]
Wenzel, Friedel [2 ]
Miny, Peter [2 ]
Zumsteg, Urs [1 ]
Heinimann, Karl [2 ]
机构：
[1] Univ Childrens Hosp, Div Pediat Endocrinol, Basel, Switzerland
[2] Dept Biomed, Div Med Genet, Basel, Switzerland
[3] Univ Hosp, Dept Obstet & Gynecol, Basel, Switzerland
来源：
SWISS MEDICAL WEEKLY | 2009年 / 139卷 / 21-22期
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D O I：
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中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
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页码：24S / 24S
页数：1
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