The phenotypic spectrum of Schaaf-Yang syndrome: 18 new affected individuals from 14 families

Author(s):
Fountain, M.D.; Aten, E.; Cho, M.T.; Juusola, J.; Walkiewicz, M.A.; Ray, J.W.; Xia, F.; Yang, Y.P.; Graham, B.H.; Bacino, C.A.; Potocki, L.; Haeringen, A. van (0000-0003-3786-6716); Ruivenkamp, C.A.L.; Mancias, P.; Northrup, H.; Kukolich, M.K.; Weiss, M.M.; Ravenswaaij-Arts, C.M.A. van; Mathijssen, I.B.; Levesque, S.; Meeks, N.; Rosenfeld, J.A.; Lemke, D.; Hamosh, A.; Lewis, S.K.; Race, S.; Stewart, L.L.; Hay, B.; Lewis, A.M.; Guerreiro, R.L.; Bras, J.T.; Martins, M.P.; Derksen-Lubsen, G.; Peeters, E.; Stumpel, C.; Stegmann, S.; Bok, L.A.; Santen, G.W.E. (0000-0003-1959-3267); Schaaf, C.P.
Published
2017
Publication type
Article / Letter to editor
MAGEL2neurodevelopmentPrader-Willi syndromeSchaaf-Yang syndrome
Date issued
2017-01-31
Language
English
Is part of
Genetics in Medicine (2017), Vol. 19, no. 1, p. 45-52
hdl
1887/116286
doi
10.1038/gim.2016.53