(Q51848110)
Statements
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BMPR1A is a candidate gene for congenital heart defects associated with the recurrent 10q22q23 deletion syndrome. (English)
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Joris R Vermeesch
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Yves Moreau
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Jeroen Breckpot
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Marijke Bauters
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Els Troost
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Koenraad Devriendt
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Hilde Van Esch
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20 October 2011
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55
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1
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12-16
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Identifiers
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