Ralph J. Florijn

Mutations in TRPM1 Are a Common Cause of Complete Congenital Stationary Night Blindness

Maria M. van Genderen, Mieke M. C. Bijveld, Y. Claassen et al. · The American Journal of Human Genetics · 2009 · 237 citations · Full text

Developmental Biology, Ophthalmology, Genetic Disorder +3

Genotype and Phenotype of 101 Dutch Patients with Congenital Stationary Night Blindness

Mieke M. C. Bijveld, Ralph J. Florijn, Arthur A. Bergen et al. · Ophthalmology · 2013 · 147 citations

Sleep, Ocular Disease, Ophthalmology +4

High-resolution DNA Fiber-FISH for genomic DNA mapping and colour bar-coding of large genes

Ralph J. Florijn, L. A. J. Bonden, Hans Vrolijk et al. · Human Molecular Genetics · 1995 · 137 citations

Autosomal Recessive Bestrophinopathy

Camiel J.F. Boon, L. Ingeborgh van den Born, Linda Visser et al. · Ophthalmology · 2013 · 121 citations

Autosomal Recessive Bestrophinopathy, Genetic Disorder, Histopathology +4

The Phenotypic Spectrum of Albinism

Charlotte C. Kruijt, Gerard C. de Wit, Arthur A. Bergen et al. · Ophthalmology · 2018 · 117 citations

Biology, Allelic Variant, Genetic Disorder +5