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Showing results (11-20 of 17) with videos related to

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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.
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.
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.
Bone|April 6, 2002
Otosclerosis: a genetically heterogeneous disease involving at least three different genesK Van Den Bogaert, P J Govaerts, E M R De Leenheer, et al.
Genomics|April 1, 1997
Linkage analysis of progressive hearing loss in five extended families maps the DFNA2 gene to a 1.25-Mb region on chromosome 1pG Van Camp, P J Coucke, H Kunst, et al.
Nature Genetics|May 20, 1998
Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairmentK Verhoeven, L Van Laer, K Kirschhofer, et al.
Human Molecular Genetics|June 17, 1999
Mutations in the KCNQ4 gene are responsible for autosomal dominant deafness in four DFNA2 familiesP J Coucke, P Van Hauwe, P M Kelley, et al.
Pageof 2

Showing results (11-20 of 17) with videos related to

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Pageof 2
You have reached the last page of results.This site can display upto 17 results.
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.
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.
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.
Bone|April 6, 2002
Otosclerosis: a genetically heterogeneous disease involving at least three different genesK Van Den Bogaert, P J Govaerts, E M R De Leenheer, et al.
Genomics|April 1, 1997
Linkage analysis of progressive hearing loss in five extended families maps the DFNA2 gene to a 1.25-Mb region on chromosome 1pG Van Camp, P J Coucke, H Kunst, et al.
Nature Genetics|May 20, 1998
Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairmentK Verhoeven, L Van Laer, K Kirschhofer, et al.
Human Molecular Genetics|June 17, 1999
Mutations in the KCNQ4 gene are responsible for autosomal dominant deafness in four DFNA2 familiesP J Coucke, P Van Hauwe, P M Kelley, et al.
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