The Koolen-de Vries syndrome: a phenotypic comparison of patients with a 17q21.31 microdeletion versus a KANSL1 sequence variant
- Author(s):
- Koolen, D.A.; Pfundt, R.; Linda, K.; Beunders, G.; Veenstra-Knol, H.E.; Conta, J.H.; Fortuna, A.M.; Gillessen-Kaesbach, G.; Dugan, S.; Halbach, S.; Abdul-Rahman, O.A.; Winesett, H.M.; Chung, W.K.; Dalton, M.; Dimova, P.S.; Mattina, T.; Prescott, K.; Zhang, H.Z.; Saal, H.M.; Hehir-Kwa, J.Y.; Willemsen, M.H.; Ockeloen, C.W.; Jongmans, M.C.; Aa, N. van der; Failla, P.; Barone, C.; Avola, E.; Brooks, A.S.; Kant, S.G.; Gerkes, E.H.; Firth, H.V.; Ounap, K.; Bird, L.M.; Masser-Frye, D.; Friedman, J.R.; Sokunbi, M.A.; Dixit, A.; Splitt, M.; Kukolich, M.K.; McGaughran, J.; Coe, B.P.; Florez, J.; Kasri, N.N.; Brunner, H.G.; Thompson, E.M.; Gecz, J.; Romano, C.; Eichler, E.E.; Vries, B.B.A. de; DDD Study
- Published
- 2016
- Publication type
- Article / Letter to editor
- Date issued
- 2016-05-31
- Language
- English
- Is part of
- European Journal of Human Genetics (2016), Vol. 24, no. 5, p. 652-659
- hdl
- 1887/112975
- doi
- 10.1038/ejhg.2015.178