Authors: Simon, A Cuisset, L Vincent, MF van der Velde-Visser, SD Delpech, M van der Meer, JWM Drenth, JPH

Citation: A. Simon et al., Molecular analysis of the mevalonate kinase gene in a cohort of patients with the hyper-IgD and periodic fever syndrome: Its application as a diagnostic tool, ANN INT MED, 135(5), 2001, pp. 338-343

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: de Kok, YJM Bom, SJH Brunt, TM Kemperman, MH van Beusekom, E van der Velde-Visser, SD Robertson, NG Morton, CC Huygen, PLM Verhagen, WIM Brunner, HG Cremers, CWRJ Cremers, FPM

Citation: Yjm. De Kok et al., A Pro51Ser mutation in the COCH gene is associated with late onset autosomal dominant progressive sensorineural hearing loss with vestibular defects, HUM MOL GEN, 8(2), 1999, pp. 361-366

Authors: den Hollander, A van der Velde-Visser, SD Pinckers, AJLG Hoyng, CB Brunner, HG Cremers, FPM

Citation: A. Den Hollander et al., Refined mapping of the gene for autosomal dominant retinitis pigmentosa (RP17) on chromosome 17q22, HUM GENET, 104(1), 1999, pp. 73-76