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American Journal of Human Genetics|February 15, 2001
A second gene for otosclerosis, OTSC2, maps to chromosome 7q34-36K Van Den Bogaert, P J Govaerts, I Schatteman, et al.American Journal of Human Genetics|May 1, 1997
A gene for autosomal dominant nonsyndromic hearing loss (DFNA12) maps to chromosome 11q22-24K Verhoeven, G Van Camp, P J Govaerts, et al.Bone|April 6, 2002
Otosclerosis: a genetically heterogeneous disease involving at least three different genesK Van Den Bogaert, P J Govaerts, E M R De Leenheer, et al.Journal of Medical Genetics|February 27, 2004
A genotype-phenotype correlation for GJB2 (connexin 26) deafnessK Cryns, E Orzan, A Murgia, et al.Nature Genetics|May 20, 1998
Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairmentK Verhoeven, L Van Laer, K Kirschhofer, et al.Plos One|November 16, 2012
Pre-, per- and postoperative factors affecting performance of postlinguistically deaf adults using cochlear implants: a new conceptual model over timeDiane S Lazard, Christophe Vincent, Frédéric Venail, et al.Ear and Hearing|February 20, 2015
A Retrospective Multicenter Study Comparing Speech Perception Outcomes for Bilateral Implantation and Bimodal RehabilitationPeter J Blamey, Bert Maat, Deniz Başkent, et al.Audiology & Neuro-Otology|October 26, 2012
Factors affecting auditory performance of postlinguistically deaf adults using cochlear implants: an update with 2251 patientsPeter Blamey, Françoise Artieres, Deniz Başkent, et al.Thescientificworldjournal|April 2, 2014
Cochlear implant programming: a global survey on the state of the artBart Vaerenberg, Cas Smits, Geert De Ceulaer, et al.Pageof 10