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G van Camp

Showing results (181-190 of 214) with videos related to

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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.
Journal of Medical Genetics|June 3, 2004
A fifth locus for otosclerosis, OTSC5, maps to chromosome 3q22-24K Van Den Bogaert, E M R De Leenheer, W Chen, et al.
Mitochondrion|June 8, 2011
Inherited mitochondrial variants are not a major cause of age-related hearing impairment in the European populationS Bonneux, E Fransen, E Van Eyken, et al.
Genome Research|October 1, 1995
An autosomal recessive nonsyndromic form of sensorineural hearing loss maps to 3p-DFNB6K Fukushima, A Ramesh, C R Srisailapathy, 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.
American Journal of Human Genetics|May 1, 1997
A gene for autosomal dominant nonsyndromic hearing loss (DFNA12) maps to chromosome 11q22-24K Verhoeven, G Van Camp, P J Govaerts, et al.
Journal of Medical Genetics|July 29, 1999
A gene for autosomal dominant hearing impairment (DFNA14) maps to a region on chromosome 4p16.3 that does not overlap the DFNA6 locusG Van Camp, H Kunst, K Flothmann, 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.
Human Mutation|May 26, 1998
Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing lossD A Scott, M L Kraft, R Carmi, et al.
European Journal of Human Genetics : EJHG|March 27, 1999
Hearing impairment and neurological dysfunction associated with a mutation in the mitochondrial tRNASer(UCN) geneK Verhoeven, R J Ensink, V Tiranti, et al.
Pageof 22

Showing results (181-190 of 214) with videos related to

Sort By:
Pageof 22
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.
Journal of Medical Genetics|June 3, 2004
A fifth locus for otosclerosis, OTSC5, maps to chromosome 3q22-24K Van Den Bogaert, E M R De Leenheer, W Chen, et al.
Mitochondrion|June 8, 2011
Inherited mitochondrial variants are not a major cause of age-related hearing impairment in the European populationS Bonneux, E Fransen, E Van Eyken, et al.
Genome Research|October 1, 1995
An autosomal recessive nonsyndromic form of sensorineural hearing loss maps to 3p-DFNB6K Fukushima, A Ramesh, C R Srisailapathy, 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.
American Journal of Human Genetics|May 1, 1997
A gene for autosomal dominant nonsyndromic hearing loss (DFNA12) maps to chromosome 11q22-24K Verhoeven, G Van Camp, P J Govaerts, et al.
Journal of Medical Genetics|July 29, 1999
A gene for autosomal dominant hearing impairment (DFNA14) maps to a region on chromosome 4p16.3 that does not overlap the DFNA6 locusG Van Camp, H Kunst, K Flothmann, 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.
Human Mutation|May 26, 1998
Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing lossD A Scott, M L Kraft, R Carmi, et al.
European Journal of Human Genetics : EJHG|March 27, 1999
Hearing impairment and neurological dysfunction associated with a mutation in the mitochondrial tRNASer(UCN) geneK Verhoeven, R J Ensink, V Tiranti, et al.
Pageof 22