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Genomics|June 30, 2000

A novel conserved cochlear gene, OTOR: identification, expression analysis, and chromosomal mappingN G Robertson, S Heller, J S Lin, et al.

Genomics|January 27, 1998

Mapping and characterization of a novel cochlear gene in human and in mouse: a positional candidate gene for a deafness disorder, DFNA9N G Robertson, A B Skvorak, Y Yin, et al.

Human Molecular Genetics|February 13, 2001

Mutations in the transcriptional activator EYA4 cause late-onset deafness at the DFNA10 locusS Wayne, N G Robertson, F DeClau, et al.

Genomics|January 7, 1998

An ancient conserved gene expressed in the human inner ear: identification, expression analysis, and chromosomal mapping of human and mouse antiquitin (ATQ1)A B Skvorak, N G Robertson, Y Yin, 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.

Nature Genetics|November 7, 1998

Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunctionN G Robertson, L Lu, S Heller, et al.

Human Molecular Genetics|February 5, 1999

A Pro51Ser mutation in the COCH gene is associated with late onset autosomal dominant progressive sensorineural hearing loss with vestibular defectsY J de Kok, S J Bom, T M Brunt, et al.

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

Sort By:

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You have reached the last page of results.This site can display upto 17 results.

Genomics|June 30, 2000

A novel conserved cochlear gene, OTOR: identification, expression analysis, and chromosomal mappingN G Robertson, S Heller, J S Lin, et al.

Genomics|January 27, 1998

Mapping and characterization of a novel cochlear gene in human and in mouse: a positional candidate gene for a deafness disorder, DFNA9N G Robertson, A B Skvorak, Y Yin, et al.

Human Molecular Genetics|February 13, 2001

Mutations in the transcriptional activator EYA4 cause late-onset deafness at the DFNA10 locusS Wayne, N G Robertson, F DeClau, et al.

Genomics|January 7, 1998

An ancient conserved gene expressed in the human inner ear: identification, expression analysis, and chromosomal mapping of human and mouse antiquitin (ATQ1)A B Skvorak, N G Robertson, Y Yin, 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.

Nature Genetics|November 7, 1998

Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunctionN G Robertson, L Lu, S Heller, et al.

Human Molecular Genetics|February 5, 1999

A Pro51Ser mutation in the COCH gene is associated with late onset autosomal dominant progressive sensorineural hearing loss with vestibular defectsY J de Kok, S J Bom, T M Brunt, et al.

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