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

页码：1054 / 1054

页数：1

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