Author: "Pondaag, W." / Journal: european journal of medical genetics - Searchworks@Jio Institute Digital Library Search Results

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Start Over Author "Pondaag, W." Journal european journal of medical genetics

1 results on '"Pondaag, W."'

1. A de novo mutation in ZMYND11, a candidate gene for 10p15.3 deletion syndrome, is associated with syndromic intellectual disability

Author: Cobben, J.M., Weiss, M.M., van Dijk, F.S., De Reuver, R., de Kruiff, C., Pondaag, W., Hennekam, R.C., and Yntema, H.G.
Published: 2014
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