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

J. Cobben, M.M. Weiss, F.S. van Dijk, R. de Reuver, C. de Kruiff, W. Pondaag, R. Hennekam, H. Yntema

Research output: Contribution to journalArticleAcademicpeer-review

Original languageUndefined/Unknown
Pages (from-to)636-638
JournalEuropean Journal of Medical Genetics
Issue number11-12
Publication statusPublished - 2014

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