Gerard van Duijnhoven
Publications by Year
Research Areas
Hearing, Cochlea, Tinnitus, Genetics, Hearing Loss and Rehabilitation, Retinal Development and Disorders, Ear Surgery and Otitis Media, Genetics and Neurodevelopmental Disorders
Most-Cited Works
- → Positional cloning of the gene for X-linked retinitis pigmentosa 2(1998)382 cited
- → A Novel Ribosomal S6-Kinase (RSK4; RPS6KA6) Is Commonly Deleted in Patients with Complex X-Linked Mental Retardation(1999)122 cited
- → A Novel Mutation Identified in the <i>DFNA5</i> Gene in a Dutch Family: A Clinical and Genetic Evaluation(2003)84 cited
- → Audiometric, Vestibular, and Genetic Aspects of a DFNA9 Family with a G88E COCH Mutation(2005)40 cited
- → Non-syndromic autosomal dominant progressive non-specific mid-frequency sensorineural hearing impairment with childhood to late adolescence onset (DFNA21)(2000)39 cited
- → Cloning, characterization, and mRNA expression analysis of novel human fetal cochlear cDNAs☆(2003)23 cited
- → A Dutch Family With Hearing Loss Linked to the DFNA20/26 Locus(2004)15 cited
- → Intrafamilial variability of the ocular phenotype in a Polish family with a missense mutation (A63D) in the Norrie disease gene(1998)13 cited
- → Linkage analysis in a Dutch family with X-linked recessive congenital stationary night blindness (XL-CSNB)(1995)10 cited
- → A Pst I Restriction Fragment Length Polymorphism near the MAO locus on Xp(1996)