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Human Molecular Genetics|October 1, 1992
Autosomal dominant branchio-oto-renal syndrome--localization of a disease gene to chromosome 8q by linkage in a Dutch familyS Kumar, W J Kimberling, J B Kenyon, et al.
Archives of Neurology|July 13, 2000
Familial progressive vestibulocochlear dysfunction caused by a COCH mutation (DFNA9)W I Verhagen, S J Bom, P L Huygen, et al.
European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|April 28, 2000
A Dutch family with progressive sensorineural hearing impairment linked to the DFNA2 regionR J Ensink, P L Huygen, P Van Hauwe, et al.
Audiology : Official Organ of the International Society of Audiology|July 24, 2001
Audiometric evaluation of bilaterally fitted bone-anchored hearing aidsA J Bosman, A F Snik, C T van der Pouw, et al.
American Journal of Medical Genetics|August 5, 2000
Mutations in the KCNQ4 K+ channel gene, responsible for autosomal dominant hearing loss, cluster in the channel pore regionP Van Hauwe, P J Coucke, R J Ensink, et al.
Clinical Otolaryngology and Allied Sciences|September 18, 2001
A Dutch family with progressive autosomal dominant non-syndromic sensorineural hearing impairment linked to DFNA13R J Ensink, P L Huygen, R L Snoeckx, et al.
International Journal of Pediatric Otorhinolaryngology|March 1, 1995
The Usher syndrome type 2A: clinical findings in obligate carriersA van Aarem, C W Cremers, A J Pinckers, et al.
Archives of Otolaryngology (Chicago, Ill. : 1960)|April 1, 1985
X-linked progressive mixed deafness with perilymphatic gusher during stapes surgeryC W Cremers, G C Hombergen, J J Scaf, et al.
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