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Explore Editage All Accesshttps://doi.org/10.1136/jmedgenet-2012-101173
Copy DOI Journal: Journal of Medical Genetics |  Publication Date: Nov 27, 2012 |
 Citations: 93 |
Affiliation: Imagine Institute for Genetic Diseases, Inserm, Université Paris Cité, Hôpital Jean-Verdier, Université Sorbonne Paris Nord, Assistance Publique – Hôpitaux de Paris, Addenbrooke's Hospital, Hôpital Necker-Enfants Malades, Sorbonne Université, Hôpital Armand-Trousseau, Hôpital d'Enfants, University of Bordeaux, Institut de Biologie de Lille, Hôpital Jeanne de Flandre, Hôpital Robert-Debré, Hôpital Saint-Vincent-de-Paul, Hôpital Maison Blanche, Centre Hospitalier Universitaire de Reims, University of Reims Champagne-Ardenne, Centre Hospitalier Universitaire de La Réunion, Hôpital Nord, Hôpital Couple Enfant, Centre Hospitalier Universitaire de GrenobleBackground:Oesophageal atresia (OA) and mandibulofacial dysostosis (MFD) are two congenital malformations for which the molecular bases of syndromic forms are being identified at a rapid rate. In particular, the EFTUD2...
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