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

Published 2011 View Full Article

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Title
BMPR1A is a candidate gene for congenital heart defects associated with the recurrent 10q22q23 deletion syndrome
Authors
Keywords
-
Journal
European Journal of Medical Genetics
Volume 55, Issue 1, Pages 12-16
Publisher
Elsevier BV
Online
2011-10-25
DOI
10.1016/j.ejmg.2011.10.003

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