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

Bibliographic Details
Title: BMPR1A is a candidate gene for congenital heart defects associated with the recurrent 10q22q23 deletion syndrome
Authors: Breckpot, Jeroen, Tranchevent, Léon-Charles, Thienpont, Bernard, Bauters, Marijke, Troost, Els, Gewillig, Marc, Vermeesch, Joris R., Moreau, Yves, Devriendt, Koenraad, Van Esch, Hilde
Source: In European Journal of Medical Genetics January 2012 55(1):12-16
Database: ScienceDirect
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ISSN:17697212
DOI:10.1016/j.ejmg.2011.10.003
Published in:European Journal of Medical Genetics
Language:English