Clinical utility gene card for: Marfan syndrome type 1 and related phenotypes [FBN1]

被引：0

作者：

Mine Arslan-Kirchner

Eloisa Arbustini

Catherine Boileau

Anne Child

Gwenaelle Collod-Beroud

Anne De Paepe

Jörg Epplen

Guillaume Jondeau

Bart Loeys

Laurence Faivre

机构：

[1] Institute of Human Genetics,Département de Génétique

[2] Hannover Medical School,Department of Human Genetics

[3] Laboratorio di Diagnostica Molecolare,undefined

[4] Patologia Cardiovascolare e dei Trapianti,undefined

[5] Centro Malattie Genetiche Cardiovascolari,undefined

[6] Policlinico San Matteo,undefined

[7] Institut de Recherche Necker Enfants Malades,undefined

[8] Hopital Necker – Enfants Malades,undefined

[9] Sonalee Laboratory,undefined

[10] Cardiac and Vascular Sciences,undefined

[11] St George's University of London,undefined

[12] Laboratoire de Génétique Moléculaire,undefined

[13] CHU de Montpellier,undefined

[14] Institut Universitaire de Recherche Clinique,undefined

[15] Center for Medical Genetics,undefined

[16] Ghent University Hospital,undefined

[17] Ruhr University Bochum,undefined

[18] Service de Cardiologie,undefined

[19] CHU Hôpital Xavier Bichat – Claude Bernard,undefined

[20] Centre de Génétique,undefined

[21] Centre Hospitalier Universitaire de Dijon,undefined

来源：

European Journal of Human Genetics | 2010年 / 18卷

关键词：

D O I：

暂无

中图分类号：

学科分类号：

摘要：

引用

页码：1071 / 1071

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