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R J Smith

Showing results (601-610 of 636) 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.
Gene|April 18, 2000
Refining the DFNB7-DFNB11 deafness locus using intragenic polymorphisms in a novel gene, TMEM2D A Scott, S Drury, R A Sundstrom, 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.
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.
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.
Genome Research|February 21, 1998
Contig maps and genomic sequencing identify candidate genes in the usher 1C locusM J Higgins, C D Day, N J Smilinich, et al.
American Journal of Medical Genetics|July 23, 1998
Localization of a novel gene for nonsyndromic hearing loss (DFNB17) to chromosome region 7q31J H Greinwald, S Wayne, A H Chen, et al.
Archives of Otolaryngology--Head & Neck Surgery|May 12, 2000
Impact of tympanostomy tubes on child quality of lifeR M Rosenfeld, M H Bhaya, C M Bower, et al.
Pageof 64

Showing results (601-610 of 636) with videos related to

Sort By:
Pageof 64
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.
Gene|April 18, 2000
Refining the DFNB7-DFNB11 deafness locus using intragenic polymorphisms in a novel gene, TMEM2D A Scott, S Drury, R A Sundstrom, 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.
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.
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.
Genome Research|February 21, 1998
Contig maps and genomic sequencing identify candidate genes in the usher 1C locusM J Higgins, C D Day, N J Smilinich, et al.
American Journal of Medical Genetics|July 23, 1998
Localization of a novel gene for nonsyndromic hearing loss (DFNB17) to chromosome region 7q31J H Greinwald, S Wayne, A H Chen, et al.
Archives of Otolaryngology--Head & Neck Surgery|May 12, 2000
Impact of tympanostomy tubes on child quality of lifeR M Rosenfeld, M H Bhaya, C M Bower, et al.
Pageof 64