Yvette J.M. de Kok

Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12)

A. Deutman, A. D. den Hollander, H. Brunner, 1999, Nature Genetics.

Isolation and mapping of novel candidate genes for retinal disorders using suppression subtractive hybridization.

A. Deutman, A. D. den Hollander, H. Brunner, 1999, Genomics.

Leber congenital amaurosis and retinitis pigmentosa with Coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (CRB1) gene.

K Rohrschneider, L I van den Born, M J van Schooneveld, 2001, American journal of human genetics.

A common ancestor for COCH related cochleovestibular (DFNA9) patients in Belgium and The Netherlands bearing the P51S mutation

C. Cremers, F. Cremers, F. Wuyts, 2001, Journal of medical genetics.