Identification of de novo variation in patients with neurodevelopmental disorder using trio whole genome sequencing

被引：0
|
作者：
Baer, Sarah [1 ,2 ]
Jeanne, Merol [1 ]
Jean-Baptiste, Lamouche [1 ]
Veronique, Geoffroy [3 ]
Alouane, Tarek [1 ]
El Chehadeh, Salima [1 ,4 ]
Skory, Valerie [1 ]
Scheidecker, Sophie [3 ,5 ]
Durand, Benjamin [4 ]
Schaefer, Elise [4 ]
Muller, Jean [3 ,5 ]
Piton, Amelie [1 ,5 ]
机构：
[1] Univ Strasbourg, Inst Genet & Mol & Cellular Biol IGBMC, INSERM, CNRS,UMR7104,U1258, Illkirch Graffenstaden, France
[2] Hop Univ Strasbourg, Pediat Neurol, Strasbourg, France
[3] Univ Strasbourg, Inst Genet Med Alsace, Federat Med Translat Strasbourg, Lab Genet Med,INSERM,U1112,UMRS 1112, Strasbourg, France
[4] Inst Genet Med Alsace, Serv Genet Clin, Strasbourg, France
[5] Hop Univ Strasbourg, Labs Diagnost Genet, Strasbourg, France
来源：
EUROPEAN JOURNAL OF HUMAN GENETICS | 2024年 / 32卷
关键词：
D O I：
暂无
中图分类号：
Q5 [生物化学]; Q7 [分子生物学];
学科分类号：
071010 ; 081704 ;
摘要：
EP10.038
引用
收藏
页码：1054 / 1054
页数：1
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