Published in

Elsevier, European Journal of Medical Genetics, 3(58), p. 140-147

DOI: 10.1016/j.ejmg.2015.01.002

Links

Tools

Export citation

Search in Google Scholar

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

Journal article published in 2015 by Clémence Vanlerberghe, Florence Petit, Valérie Malan, Catherine Vincent-Delorme, Sonia Bouquillon, Odile Boute, Muriel Holder-Espinasse, Bruno Delobel, Bénédicte Duban, Louis Vallee, Jean-Marie Cuisset, Marie-Pierre Lemaitre, Marie-Christine Vantyghem, Marie Pigeyre ORCID, Sandrine Lanco-Dosen and other authors.
This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

Full text: Unavailable

Green circle
Preprint: archiving allowed
Upload
Orange circle
Postprint: archiving restricted
Upload
Red circle
Published version: archiving forbidden
Policy details
Data provided by SHERPA/RoMEO