BMPR1A is a candidate gene for congenital heart defects associated with the recurrent 10q22q23 deletion syndrome
Title: | BMPR1A is a candidate gene for congenital heart defects associated with the recurrent 10q22q23 deletion syndrome |
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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 |
ISSN: | 17697212 |
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DOI: | 10.1016/j.ejmg.2011.10.003 |
Published in: | European Journal of Medical Genetics |
Language: | English |