Holoprosencephaly: variation of expression in face and brain in three sibs.

Por Zwetsloot, C P, Brouwer, O F, Maaswinkel-Mooy, P D
Publicado em 1989

Clinical course of untreated tonic-clonic seizures in childhood: prospective, hospital based study.

Por van Donselaar, C. A., Brouwer, O. F., Geerts, A. T., Arts, W. F., Stroink, H., Peters, A. C.
Publicado em 1997

Oculoauriculovertebral spectrum and cerebral anomalies.

Por Schrander-Stumpel, C T, de Die-Smulders, C E, Hennekam, R C, Fryns, J P, Bouckaert, P X, Brouwer, O F, da Costa, J J, Lommen, E J, Maaswinkel-Mooy, P D
Publicado em 1992

Genetic linkage map of facioscapulohumeral muscular dystrophy and five polymorphic loci on chromosome 4q35-qter

Por Wijmenga, C., Sandkuijl, L. A., Moerer, P., van der Boorn, N., Bodrug, S. E., Ray, P. N., Brouwer, O. F., Murray, J. C., van Ommen, G. J. B., Padberg, G. W., Frants, R. R.
Publicado em 1992

Immunoglobulins in children with epilepsy: the Dutch Study of Epilepsy in Childhood

Por CALLENBACH, P M C, JOL-VAN DER ZIJDE, C M, GEERTS, A T, ARTS, W F M, VAN DONSELAAR, C A, PETERS, A C B, STROINK, H, BROUWER, O F, VAN TOL, M J D
Publicado em 2003

Male patients affected by mosaic PCDH19 mutations: five new cases

Por de Lange, I. M., Rump, P., Neuteboom, R. F., Augustijn, P. B., Hodges, K., Kistemaker, A. I., Brouwer, O. F., Mancini, G. M. S., Newman, H. A., Vos, Y. J., Helbig, K. L., Peeters-Scholte, C., Kriek, M., Knoers, N. V., Lindhout, D., Koeleman, B. P. C., van Kempen, M. J. A., Brilstra, E. H.
Publicado no Neurogenetics (2017)