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American Journal of Audiology|January 26, 2000
Connexin 26 as a cause of hereditary hearing lossW T McGuirt, R J SmithAmerican Journal of Medical Genetics|March 7, 2000
Autosomal dominant nonsyndromic hearing impairmentL Van Laer, W T McGuirt, T Yang, et al.Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery|December 1, 1995
Consumption of a high-galactose diet induces diabetic-like changes in the inner earE Raynor, W G Robison, C G Garrett, et al.International Journal of Radiation Oncology, Biology, Physics|April 1, 1997
Definitive radiotherapy for early glottic carcinoma: prognostic factors and implications for treatmentL S Burke, K M Greven, W T McGuirt, et al.International Journal of Radiation Oncology, Biology, Physics|July 15, 1997
Definitive radiotherapy for early glottic carcinoma: prognostic factors and implications for treatmentL S Burke, K M Greven, W T McGuirt, et al.The Laryngoscope|February 19, 2000
Temporal bone histopathology in connexin 26-related hearing lossA I Jun, W T McGuirt, R Hinojosa, et al.Archives of Otolaryngology--Head & Neck Surgery|February 15, 2001
Autosomal dominant inherited hearing impairment caused by a missense mutation in COL11A2 (DFNA13)E M De Leenheer, H H Kunst, W T McGuirt, et al.American Journal of Human Genetics|June 12, 1999
A gene for fluctuating, progressive autosomal dominant nonsyndromic hearing loss, DFNA16, maps to chromosome 2q23-24.3K Fukushima, N Kasai, Y Ueki, et al.Human Molecular Genetics|March 21, 1998
Localization of a gene for otosclerosis to chromosome 15q25-q26M S Tomek, M R Brown, S R Mani, et al.Human Molecular Genetics|July 13, 1999
High prevalence of symptoms of Menière's disease in three families with a mutation in the COCH geneE Fransen, M Verstreken, W I Verhagen, et al.Pageof 2