Movement disorder and neuronal migration disorder due to ARFGEF2 mutation

Por de Wit, M. C. Y., de Coo, I. F. M., Halley, D. J. J., Lequin, M. H., Mancini, G. M. S.
Publicado em 2009

Interdependence of clinical factors predicting cognition in children with tuberous sclerosis complex

Por Overwater, I. E., Verhaar, B. J. H., Lingsma, H. F., Bindels-de Heus, G. C. B., van den Ouweland, A. M. W., Nellist, M., ten Hoopen, L. W., Elgersma, Y., Moll, H. A., de Wit, M. C. Y.
Publicado no J Neurol (2016)

Distinctive Phenotypic Abnormalities Associated with Submicroscopic 21q22 Deletion Including DYRK1A

Por Oegema, R., de Klein, A., Verkerk, A.J., Schot, R., Dumee, B., Douben, H., Eussen, B., Dubbel, L., Poddighe, P.J., van der Laar, I., Dobyns, W.B., van der Spek, P.J., Lequin, M.H., de Coo, I.F.M., de Wit, M.-C.Y., Wessels, M.W., Mancini, G.M.S.
Publicado em 2010