Genetic basis of Y-linked hearing impairment. - Wikidata - awgldk - TriplyDB

Genetic basis of Y-linked hearing impairment.

Genetic basis of Y-linked hearing impairment.

http://www.wikidata.org/entity/Q34324539

about

Genetics of Tinnitus: Still in its Infancy.Transmembrane channel-like (TMC) genes are required for auditory and vestibular mechanosensation.Copy number variation in the human Y chromosome in the UK population.Genetics of cardiovascular disease: Importance of sex and ethnicity.Genotype phenotype correlations for hearing impairment: approaches to management.Genetic investigations in childhood deafness.Clinical and laboratory features of cats with feline infectious peritonitis--a retrospective study of 231 confirmed cases (2000-2010).Republished: Genetic investigations in childhood deafness.Human Y-chromosome variation in the genome-sequencing era.

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Genetic basis of Y-linked hearing impairment.

http://www.wikidata.org/entity/Q34324539

description

2013 nî lūn-bûn

@nan

2013 թուականի Յունուարին հրատարակուած գիտական յօդուած

@hyw

2013 թվականի հունվարին հրատարակված գիտական հոդված

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2013年の論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年论文

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name

Genetic basis of Y-linked hearing impairment.

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Genetic basis of Y-linked hearing impairment.

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Genetic basis of Y-linked hearing impairment.

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type

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Genetic basis of Y-linked hearing impairment.

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Genetic basis of Y-linked hearing impairment.

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Genetic basis of Y-linked hearing impairment.

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Genetic basis of Y-linked hearing impairment.

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Genetic basis of Y-linked hearing impairment.

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Genetic basis of Y-linked hearing impairment.

@nl

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J.AJHG.2012.12.015

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American Journal of Human Genetics

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Genetic basis of Y-linked hearing impairment.

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Asan

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Bee Ling Ng

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Ciara Fahey

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Daniel J Turner

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Dongyi Han

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Fengtang Yang

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John Burton

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Matthew E Hurles

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Nigel P Carter

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Qingjie Liu

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P2860

Three-dimensional maps of all chromosomes in human male fibroblast nuclei and prometaphase rosettes.

Structural variation on the short arm of the human Y chromosome: recurrent multigene deletions encompassing Amelogenin Y

Paired-end mapping reveals extensive structural variation in the human genome

The male-specific region of the human Y chromosome is a mosaic of discrete sequence classes

The human Y chromosome: an evolutionary marker comes of age

Human Y chromosome base-substitution mutation rate measured by direct sequencing in a deep-rooting pedigree

SSAHA: a fast search method for large DNA databases

DFNA49, a novel locus for autosomal dominant non-syndromic hearing loss, maps proximal to DFNA7/DFNM1 region on chromosome 1q21-q23.

A microhomology-mediated break-induced replication model for the origin of human copy number variation.

2003 Curt Stern Award address. On low expectation exceeded; or, the genomic salvation of the Y chromosome

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Michael Andrew Quail

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