Show 10 5 10 15 20 50 100 250 Sort by year (new to old) Actions Download search results Subscribe to news feed Your filters: cql: author="Cremers, FPM" or (type any "bookEditor journalEditor issueEditor" and editor="Cremers, FPM") Add to list Journal Article A1 Mutations in GRM6 cause autosomal recessive congenital stationary night blindness with a distinctive scotopic 15-Hz flicker electroretinogram C ZEITZ, M VAN GENDEREN, J NEIDHARDT, UFO LUHMANN, F HOEBEN, U FORSTER, K WYCISK, G MATYAS, CB HOYNG, F RIEMSLAG, et al. (2005) INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE. 46(11). p.4328-4335 Add to list Journal Article A1 A novel mutation in the ELOVL4 gene causes autosomal dominant Stargardt-like macular dystrophy A MAUGERI, Françoise Meire (UGent) , CB HOYNG, C VINK, N VAN REGEMORTER, G KARAN, ZL YANG, FPM CREMERS and Kaibo Zhang (2004) INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE. 45(12). p.4263-4267 Add to list Journal Article A1 A novel mutation identified in the DFNA5 gene in a Dutch family: A clinical and genetic evaluation AMLC Bischoff, MWJ Luijendijk, PLM Huygen, G van Duijnhoven, Els De Leenheer (UGent) , GG Oudesluijs, Lut Van Laer (UGent) , FPM Cremers, CWRJ Cremers and H Kremer (2004) AUDIOLOGY AND NEURO-OTOLOGY. 9(1). p.34-46