Xq28 duplications including MECP2 in five females: Expanding the phenotype to severe mental retardation

Author(s):
Bijlsma, E.K.; Collins, A.; Papa, F.T.; Tejada, M.I.; Wheeler, P.; Peeters, E.A.J.; Gijsbers, A.C.J.; Kamp, J.M.V. de; Kriek, M.; Losekoot, M.; Broekma, A.J.; Crolla, J.A.; Pollazzon, M.; Mucciolo, M.; Katzaki, E.; Disciglio, V.; Ferreri, M.I.; Marozza, A.; Mencarelli, M.A.; Castagnini, C.; Dosa, L.; Ariani, F.; Mari, F.; Canitano, R.; Hayek, G.; Botella, M.P.; Gener, B.; Minguez, M.; Renieri, A.; Ruivenkamp, C.A.L.
Published
2012
Publication type
Article / Letter to editor
MECP2 duplicationXq28 duplicationX-inactivationMental retardation in femalesIRAK1
Date issued
2012-07-31
Language
English
Is part of
European Journal of Medical Genetics (2012), Vol. 55, no. 6-7, p. 404-413
hdl
1887/97744
doi
10.1016/j.ejmg.2012.02.009