Genomic imbalances in mental retardation

le Kriek, M, White, S, Bouma, M, Dauwerse, H, Hansson, K, Nijhuis, J, Bakker, B, van Ommen, G-J B, den Dunnen, J T, Breuning, M
Foilsithe 2004

Cerebral White Matter Abnormalities in 6p25 Deletion Syndrome

le van der Knaap, M.S., Kriek, M., Overweg-Plandsoen, W.C.G., Hansson, K.B., Madan, K., Starreveld, J.S., Schotman-Schram, P., Barkhof, F., Oberstein, S.A.M.J. Lesnik
Foilsithe in AJNR Am J Neuroradiol (2006)

Array‐CGH detection of micro rearrangements in mentally retarded individuals: clinical significance of imbalances present both in affected children and normal parents

le Rosenberg, C, Knijnenburg, J, Bakker, E, Vianna‐Morgante, A M, Sloos, W, Otto, P A, Kriek, M, Hansson, K, Krepischi‐Santos, A C V, Fiegler, H, Carter, N P, Bijlsma, E K, van Haeringen, A, Szuhai, K, Tanke, H J
Foilsithe 2006

Male patients affected by mosaic PCDH19 mutations: five new cases

le 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.
Foilsithe in Neurogenetics (2017)

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

le Bijlsma, E.K., Collins, A., Papa, F.T., Tejada, M.I., Wheeler, P., Peeters, E.A.J., Gijsbers, A.C.J., van de Kamp, J.M., 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., Mínguez, M., Renieri, A., Ruivenkamp, C.A.L.
Foilsithe 2012