A novel locus for autosomal dominant non-syndromic deafness, DFNA53, maps to chromosome 14q11.2-q12.

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The genetic bases for non-syndromic hearing loss among Chinese c.G2114A MYH9 mutation (DFNA17) causes non-syndromic autosomal dominant hearing loss in a Brazilian family.Polymorphism of the 86th amino acid in CX26 protein and hereditary deafness.

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P2860

A novel locus for autosomal dominant non-syndromic deafness, DFNA53, maps to chromosome 14q11.2-q12.

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2005 nî lūn-bûn

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A novel locus for autosomal do ...... aps to chromosome 14q11.2-q12.

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A novel locus for autosomal do ...... aps to chromosome 14q11.2-q12.

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A novel locus for autosomal do ...... aps to chromosome 14q11.2-q12.

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A novel locus for autosomal do ...... aps to chromosome 14q11.2-q12.

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A novel locus for autosomal do ...... aps to chromosome 14q11.2-q12.

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A novel locus for autosomal do ...... aps to chromosome 14q11.2-q12.

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A novel locus for autosomal do ...... aps to chromosome 14q11.2-q12.

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D Yan

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L L Du

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S H Blanton

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P2860

PedCheck: a program for identification of genotype incompatibilities in linkage analysis

A novel locus (DFNA23) for prelingual autosomal dominant nonsyndromic hearing loss maps to 14q21-q22 in a Swiss German kindred

Strategies for multilocus linkage analysis in humans

Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunction

High prevalence of symptoms of Menière's disease in three families with a mutation in the COCH gene

Mutations in the COCH gene are a frequent cause of autosomal dominant progressive cochleo-vestibular dysfunction, but not of Meniere's disease

Identification of a novel COCH mutation, I109N, highlights the similar clinical features observed in DFNA9 families

A gene for non-syndromic autosomal dominant progressive postlingual sensorineural hearing loss maps to chromosome 14q12-13

A Pro51Ser mutation in the COCH gene is associated with late onset autosomal dominant progressive sensorineural hearing loss with vestibular defects

Autosomal dominant sensorineural hearing loss. Pedigrees, audiologic findings, and temporal bone findings in two kindreds

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A novel locus for autosomal dominant non-syndromic deafness, DFNA53, maps to chromosome 14q11.2-q12.

about

P2860

P2860

A novel locus for autosomal dominant non-syndromic deafness, DFNA53, maps to chromosome 14q11.2-q12.

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