BMPR1A is a candidate gene for congenital heart defects associated with the recurrent 10q22q23 deletion syndrome
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| Description | scientific article published on 20 October 2011 |
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author: Yves Moreau Bernard Thienpont Joris R Vermeesch Léon-Charles Tranchevent Marc Gewillig |
| Publication date | October 20, 2011 |
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