Further delineation of the KBG syndrome phenotype caused by ANKRD11 aberrations
- Author(s):
- 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.
- Published
- 2015
- Publication type
- Article / Letter to editor
- Date issued
- 2015-09-30
- Language
- English
- Is part of
- European Journal of Human Genetics (2015), Vol. 23, no. 9, p. 1176-1185
- hdl
- 1887/105737
- doi
- 10.1038/ejhg.2014.253