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Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|March 27, 2015
A Retrospective Cohort Study on the Influence of Comorbidity on Soft Tissue Reactions, Revision Surgery, and Implant Loss in Bone-anchored Hearing ImplantsChristine A den Besten, Rik C Nelissen, Petronella G M Peer, et al.Human Molecular Genetics|January 26, 2006
The DFNB31 gene product whirlin connects to the Usher protein network in the cochlea and retina by direct association with USH2A and VLGR1Erwin van Wijk, Bert van der Zwaag, Theo Peters, et al.Human Molecular Genetics|February 17, 2006
Cochlin immunostaining of inner ear pathologic deposits and proteomic analysis in DFNA9 deafness and vestibular dysfunctionNahid G Robertson, Cor W R J Cremers, Patrick L M Huygen, et al.Journal of the Association for Research in Otolaryngology : JARO|July 26, 2011
Genotype-phenotype correlation in DFNB8/10 families with TMPRSS3 mutationsNicole J D Weegerink, Margit Schraders, Jaap Oostrik, et al.Orphanet Journal of Rare Diseases|December 31, 2011
Osteogenesis Imperfecta: the audiological phenotype lacks correlation with the genotypeFreya K R Swinnen, Paul J Coucke, Anne M De Paepe, et al.Human Mutation|July 9, 2004
USH2A mutation analysis in 70 Dutch families with Usher syndrome type IIRonald J E Pennings, Heleen Te Brinke, Michael D Weston, et al.American Journal of Human Genetics|February 24, 2009
A genome-wide analysis identifies genetic variants in the RELN gene associated with otosclerosisIsabelle Schrauwen, Megan Ealy, Matthew J Huentelman, et al.American Journal of Medical Genetics. Part A|September 14, 2007
MYO15A (DFNB3) mutations in Turkish hearing loss families and functional modeling of a novel motor domain mutationErsan Kalay, Abdullah Uzumcu, Elmar Krieger, et al.American Journal of Human Genetics|February 9, 2010
Homozygosity mapping reveals mutations of GRXCR1 as a cause of autosomal-recessive nonsyndromic hearing impairmentMargit Schraders, Kwanghyuk Lee, Jaap Oostrik, et al.Human Mutation|March 22, 2007
Involvement of DFNB59 mutations in autosomal recessive nonsyndromic hearing impairmentRob W J Collin, Ersan Kalay, Jaap Oostrik, et al.Pageof 18