15q11.2 microdeletion (BP1–BP2) and developmental delay, behaviour issues, epilepsy and congenital heart disease: A series of 52 patients-Reference-Cited by-同舟云学术

15q11.2 microdeletion (BP1–BP2) and developmental delay, behaviour issues, epilepsy and congenital heart disease: A series of 52 patients

Published:2015-03 Issue:3 Volume:58 Page:140-147
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Vanlerberghe Clémence,Petit Florence,Malan Valérie,Vincent-Delorme Catherine,Bouquillon Sonia,Boute Odile,Holder-Espinasse Muriel,Delobel Bruno,Duban Bénédicte,Vallee Louis,Cuisset Jean-Marie,Lemaitre Marie-Pierre,Vantyghem Marie-Christine,Pigeyre Marie,Lanco-Dosen Sandrine,Plessis Ghislaine,Gerard Marion,Decamp Matthieu,Mathieu Michèle,Morin Gilles,Jedraszak Guillaume,Bilan Frédéric,Gilbert-Dussardier Brigitte,Fauvert Delphine,Roume Joëlle,Cormier-Daire Valérie,Caumes Roseline,Puechberty Jacques,Genevieve David,Sarda Pierre,Pinson Lucie,Blanchet Patricia,Lemeur Nathalie,Sheth Frenny^ORCID,Manouvrier-Hanu Sylvie,Andrieux Joris

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics,General Medicine

Reference49 articles.

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