Gerard van Duijnhoven

Positional cloning of the gene for X-linked retinitis pigmentosa 2

Uwe Schwahn, Steffen Lenzner, Juan Dong et al. · Nature Genetics · 1998 · 381 citations

Natural Sciences, Genetics, Genomic Mechanism +10

A Novel Ribosomal S6-Kinase (RSK4; RPS6KA6) Is Commonly Deleted in Patients with Complex X-Linked Mental Retardation

Helger G. Yntema, Bellinda van den Helm, J. Kissing et al. · Genomics · 1999 · 122 citations

Novel Ribosomal S6-kinase, Chromatin, Genetic Disorder +5

A Novel Mutation Identified in the <i>DFNA5</i> Gene in a Dutch Family: A Clinical and Genetic Evaluation

Anne M.L.C. Bischoff, Mirjam W.J. Luijendijk, P.L.M. Huygen et al. · Audiology and Neurotology · 2003 · 84 citations

Audiometric, Vestibular, and Genetic Aspects of a DFNA9 Family with a G88E COCH Mutation

Martijn H. Kemperman, Els De Leenheer, P.L.M. Huygen et al. · Otology & Neurotology · 2005 · 40 citations

Non-syndromic autosomal dominant progressive non-specific mid-frequency sensorineural hearing impairment with childhood to late adolescence onset (DFNA21)

Henricus P. M. Kunst, Henri A. M. Marres, P.L.M. Huygen et al. · Clinical Otolaryngology · 2000 · 39 citations

Family Members, Offset Threshold, Noise +18