Holt-Oram syndrome: clinical and molecular insights

被引：0

作者：

Vanlerberghe, C. ^{[1
,2
]}

Jourdain, A. ^{[2
,3
]}

Ghoumid, J. ^{[1
,2
]}

Frenois, F. ^{[2
]}

Mezel, A. ^{[4
]}

Vaksmann, G. ^{[5
]}

Lenne, B. ^{[6
]}

Delobel, B. ^{[6
]}

Porchet, N. ^{[3
]}

Cormier-Daire, V. ^{[7
]}

Petit, F. ^{[1
,2
]}

Escande, F. ^{[2
,3
]}

Manouvrier, S. ^{[1
,2
]}

机构：

[1] CHU Lille, Dept Clin Genet, Lille, France

[2] Univ Lille, RADEME, EA 7364, Lille, France

[3] CHU Lille, Inst Biochim & Genet Mol, Lille, France

[4] CHU Lille, Unite Chirurg Orthoped Infantile, Lille, France

[5] Cabinet Vendome Cardio, Ctr Cardiol Infantile, Lille, France

[6] Hop St Vincent de Paul, Ctr Genet Chromosom, Lille, France

[7] Hop Necker Enfants Malad, AP HP, Fdn Imagine, Serv Genet,U781, Paris, France

来源：

EUROPEAN JOURNAL OF HUMAN GENETICS | 2018年 / 26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：

P04.28D

引用

页码：229 / 230

页数：2

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