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B-ENT|January 30, 2008
Prevalence of tinnitus and audiometric shapeK Demeester, A van Wieringen, J J Hendrickx, et al.Journal of Medical Genetics|June 3, 2004
DFNA5: hearing impairment exon instead of hearing impairment gene?L Van Laer, K Vrijens, S Thys, et al.Human Mutation|August 19, 2006
KCNQ4: a gene for age-related hearing impairment?E Van Eyken, L Van Laer, E Fransen, et al.Human Molecular Genetics|November 1, 1995
Localization of a gene for non-syndromic hearing loss (DFNA5) to chromosome 7p15G van Camp, P Coucke, W Balemans, et al.Genes and Immunity|February 26, 2010
Involvement of T-cell receptor-beta alterations in the development of otosclerosis linked to OTSC2I Schrauwen, K Venken, K Vanderstraeten, et al.The American Journal of Cardiology|January 17, 2021
Effect of Mitral Regurgitation on Thrombotic Risk in Patients With Nonrheumatic Atrial Fibrillation: A New CHA<sub>2</sub>DS<sub>2</sub>-VASc Score Risk Modifier?Sven L Van Laer, Seppe Verreyen, Koen M Winkler, et al.Frontiers in Cardiovascular Medicine|June 19, 2026
Titin modulation and left ventricular remodelling in chronic primary mitral regurgitationLobke L Pype, Melissa Herwig, Sven L Van Laer, et al.Human Molecular Genetics|June 1, 1996
A gene for autosomal dominant late-onset progressive non-syndromic hearing loss, DFNA10, maps to chromosome 6M E O'Neill, J Marietta, D Nishimura, et al.European Journal of Human Genetics : EJHG|February 5, 1998
Refined mapping of a gene for autosomal dominant progressive sensorineural hearing loss (DFNA5) to a 2-cM region, and exclusion of a candidate gene that is expressed in the cochleaL Van Laer, G Van Camp, D van Zuijlen, et al.Annals of Human Genetics|February 3, 2009
Candidate gene association study for noise-induced hearing loss in two independent noise-exposed populationsA Konings, L Van Laer, A Wiktorek-Smagur, et al.Pageof 5