Persistent URL of this record https://hdl.handle.net/1887/105359
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A de novo mutation in ZMYND11, a candidate gene for 10p15.3 deletion syndrome, is associated with syndromic intellectual disability
- All authors
- Cobben, J.M.; Weiss, M.M.; Dijk, F.S. van; Reuver, R. de; Kruiff, C. de; Pondaag, W.; Hennekam, R.C.; Yntema, H.G.
- Date
- 2014-12-31
- Volume
- 57
- Issue
- 11-12
- Pages
- 636 - 638