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BMPR1A is a candidate gene for congenital heart defects associated with the recurrent 10q22q23 deletion syndrome

✍ Scribed by Jeroen Breckpot; Léon-Charles Tranchevent; Bernard Thienpont; Marijke Bauters; Els Troost; Marc Gewillig; Joris R. Vermeesch; Yves Moreau; Koenraad Devriendt; Hilde Van Esch

Book ID: 116433430
Publisher: Elsevier Science
Year: 2012
Tongue: English
Weight: 306 KB
Volume: 55
Category: Article
ISSN: 1769-7212
DOI: 10.1016/j.ejmg.2011.10.003

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