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G van Camp

Showing results (171-180 of 214) with videos related to

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Human Molecular Genetics|June 1, 1996
A gene for autosomal dominant late-onset progressive non-syndromic hearing loss, DFNA10, maps to chromosome 6M E O'Neill, J Marietta, D Nishimura, et al.
The American Journal of Otology|September 19, 2000
Audiometric analysis of a Belgian family linked to the DFNA10 locusM Verstreken, F Declau, I Schatteman, et al.
American Journal of Medical Genetics|September 5, 1997
New gene for autosomal recessive non-syndromic hearing loss maps to either chromosome 3q or 19pA Chen, S Wayne, A Bell, 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.
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.
European Journal of Human Genetics : EJHG|February 5, 1998
Refined mapping of a gene for autosomal dominant progressive sensorineural hearing loss (DFNA5) to a 2-cM region, and exclusion of a candidate gene that is expressed in the cochleaL Van Laer, G Van Camp, D van Zuijlen, et al.
Annals of Human Genetics|February 3, 2009
Candidate gene association study for noise-induced hearing loss in two independent noise-exposed populationsA Konings, L Van Laer, A Wiktorek-Smagur, et al.
Journal of Medical Genetics|June 30, 2000
Identification of two different mutations in the PDS gene in an inbred family with Pendred syndromeP J Coucke, P Van Hauwe, L A Everett, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|November 8, 2001
Hereditary otovestibular dysfunction and Ménière's disease in a large Belgian family is caused by a missense mutation in the COCH geneM Verstreken, F Declau, F L Wuyts, et al.
Nature Genetics|March 18, 1999
Deafness linked to DFNA2: one locus but how many genes?P Van Hauwe, P J Coucke, F Declau, et al.
Pageof 22

Showing results (171-180 of 214) with videos related to

Sort By:
Pageof 22
Human Molecular Genetics|June 1, 1996
A gene for autosomal dominant late-onset progressive non-syndromic hearing loss, DFNA10, maps to chromosome 6M E O'Neill, J Marietta, D Nishimura, et al.
The American Journal of Otology|September 19, 2000
Audiometric analysis of a Belgian family linked to the DFNA10 locusM Verstreken, F Declau, I Schatteman, et al.
American Journal of Medical Genetics|September 5, 1997
New gene for autosomal recessive non-syndromic hearing loss maps to either chromosome 3q or 19pA Chen, S Wayne, A Bell, 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.
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.
European Journal of Human Genetics : EJHG|February 5, 1998
Refined mapping of a gene for autosomal dominant progressive sensorineural hearing loss (DFNA5) to a 2-cM region, and exclusion of a candidate gene that is expressed in the cochleaL Van Laer, G Van Camp, D van Zuijlen, et al.
Annals of Human Genetics|February 3, 2009
Candidate gene association study for noise-induced hearing loss in two independent noise-exposed populationsA Konings, L Van Laer, A Wiktorek-Smagur, et al.
Journal of Medical Genetics|June 30, 2000
Identification of two different mutations in the PDS gene in an inbred family with Pendred syndromeP J Coucke, P Van Hauwe, L A Everett, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|November 8, 2001
Hereditary otovestibular dysfunction and Ménière's disease in a large Belgian family is caused by a missense mutation in the COCH geneM Verstreken, F Declau, F L Wuyts, et al.
Nature Genetics|March 18, 1999
Deafness linked to DFNA2: one locus but how many genes?P Van Hauwe, P J Coucke, F Declau, et al.
Pageof 22