Persistent URL of this record https://hdl.handle.net/1887/105737
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![Further delineation of the KBG syndrome phenotype caused by ANKRD11 aberrations](https://scholarlypublications.universiteitleiden.nl/sites/all/themes/scholarly/img/closed_access.png)
Further delineation of the KBG syndrome phenotype caused by ANKRD11 aberrations
- All authors
- Ockeloen, C.W.; Willemsen, M.H.; Munnik, S. de; Bon, B.W.M. van; Leeuw, N. de; Verrips, A.; Kant, S.G.; Jones, E.A.; Brunner, H.G.; Loon, R.L.E. van; Smeets, E.E.J.; Haelst, M.M. van; Haaften, G. van; Nordgren, A.; Malmgren, H.; Grigelioniene, G.; Vermeer, S.; Louro, P.; Ramos, L.; Maal, T.J.J.; Heumen, C.C. van; Yntema, H.G.; Carels, C.E.L.; Kleefstra, T.
- Date
- 2015-09-30
- Volume
- 23
- Issue
- 9
- Pages
- 1176 - 1185