Authors: den Hollander, AI Heckenlively, JR van den Born, LI de Kok, YJM van der Velde-Visser, SD Kellner, U Jurklies, B van Schooneveld, MJ Blankenagel, A Rohrschneider, K Wissinger, B Cruysberg, JRM Deutman, AF Brunner, HG Apfeldstedt-Sylla, E Hoyng, CB Cremers, FPM

Citation: Ai. Den Hollander et al., Leber congenital amaurosis and retinitis pigmentosa with coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (CRB1) gene, AM J HU GEN, 69(1), 2001, pp. 198-203

Authors: Muller, D Hoenderop, JGJ Meij, IC van den Heuvel, LPJ Knoers, NVAM den Hollander, AI Eggert, P Garcia-Nieto, V Claverie-Martin, F Bindels, RJM

Citation: D. Muller et al., Molecular cloning, tissue distribution, and chromosomal manning of the human epithelial Ca2+ channel (ECAC1), GENOMICS, 67(1), 2000, pp. 48-53

Authors: den Hollander, AI ten Brink, JB de Kok, YJM van Soest, S van den Born, LI van Driel, MA van de Pol, DJR Payne, AM Bhattacharya, SS Kellner, U Hoyng, CB Westerveld, A Brunner, HG Bleeker-Wagemakers, EM Deutman, AF Heckenlively, JR Cremers, FPM Bergen, AAB

Citation: Ai. Den Hollander et al., Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12), NAT GENET, 23(2), 1999, pp. 217-221

Authors: den Hollander, AI van Driel, MA de Kok, YJM van de Pol, DJR Hoyng, CB Brunner, HG Deutman, AF Cremers, FPM

Citation: Ai. Den Hollander et al., Isolation and mapping of novel candidate genes for retinal disorders usingsuppression subtractive hybridization, GENOMICS, 58(3), 1999, pp. 240-249