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

被引：0
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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
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页码：1071 / 1071
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