Showing results (131-140 of 158) with videos related to
Sort By:
Pageof 16
The Laryngoscope|September 28, 1999
Progressive cochleovestibular impairment caused by a point mutation in the COCH gene at DFNA9S J Bom, M H Kemperman, Y J De Kok, 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|January 1, 1995
Gene mapping of Usher syndrome type IIa: localization of the gene to a 2.1-cM segment on chromosome 1q41W J Kimberling, M D Weston, C Möller, et al.American Journal of Medical Genetics|September 25, 1995
Phenotypic manifestations of branchio-oto-renal syndromeA Chen, M Francis, L Ni, et al.Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|November 8, 2001
Clinical experience with the Vibrant Soundbridge implant deviceU Fisch, C W Cremers, T Lenarz, et al.American Journal of Human Genetics|June 13, 2001
A common ancestral origin of the frequent and widespread 2299delG USH2A mutationB Dreyer, L Tranebjaerg, V Brox, et al.Archives of Otolaryngology--Head & Neck Surgery|August 26, 1998
Early-onset sensorineural hearing loss and late-onset neurologic complaints caused by a mitochondrial mutation at position 7472R J Ensink, K Verhoeven, H A Marres, et al.Leukemia Research|January 1, 1983
Purine metabolism in childhood acute lymphoblastic leukemia: biochemical markers for diagnosis and chemotherapyJ P van Laarhoven, G T Spierenburg, J A Bakkeren, et al.International Journal of Pediatric Otorhinolaryngology|December 16, 1998
Progressive hearing loss, hypoplasia of the cochlea and widened vestibular aqueducts are very common features in Pendred's syndromeC W Cremers, R J Admiraal, P L Huygen, et al.The New England Journal of Medicine|August 18, 1994
Linkage of autosomal dominant hearing loss to the short arm of chromosome 1 in two familiesP Coucke, G Van Camp, B Djoyodiharjo, et al.Pageof 16