Y J de Kok

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.

Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4

M Bitner-Glindzicz, M. Bitner-Glindzicz, H. Ropers, 1995, Science.

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

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