(Q36374800)

13 August 2017

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title

An overview of hereditary hearing loss (English)

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13 August 2017

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Yildirim A Bayazit

1

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13 August 2017

Metin Yilmaz

series ordinal

2

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13 August 2017

publication date

20 January 2006

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13 August 2017

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13 August 2017

volume

68

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13 August 2017

issue

2

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13 August 2017

page(s)

57-63

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Advances in hereditary deafness

13 August 2017

cites work

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GJB2 gene mutations causing familial hereditary deafness in Turkey.

21 January 2018

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Genetics and molecular biology of deafness

21 January 2018

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Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

21 January 2018

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Clinical features of the prevalent form of childhood deafness, DFNB1, due to a connexin-26 gene defect: implications for genetic counselling.

21 January 2018

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Mutations in the connexin 26 gene (GJB2) among Ashkenazi Jews with nonsyndromic recessive deafness

21 January 2018

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Prevalent connexin 26 gene (GJB2) mutations in Japanese

21 January 2018

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Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans

21 January 2018

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Novel mutations in the connexin 26 gene (GJB2) that cause autosomal recessive (DFNB1) hearing loss

21 January 2018

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Two different connexin 26 mutations in an inbred kindred segregating non-syndromic recessive deafness: implications for genetic studies in isolated populations.

21 January 2018

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Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 gene

21 January 2018

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Connexin-26 mutations in sporadic and inherited sensorineural deafness

21 January 2018

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Connexin mutations and hearing loss.

21 January 2018

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Clinical diagnosis of the Usher syndromes. Usher Syndrome Consortium

21 January 2018

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Pendred syndrome--100 years of underascertainment?

21 January 2018

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A mutation in PDS causes non-syndromic recessive deafness

21 January 2018

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Molecular basis of the long-QT syndrome associated with deafness

21 January 2018

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21 January 2018

The genetics of deafness

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A human homologue of the Drosophila eyes absent gene underlies branchio-oto-renal (BOR) syndrome and identifies a novel gene family

21 January 2018

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Oto- spondylo-megaepiphyseal dysplasia (OSMED): clinical description of three patients homozygous for a missense mutation in the COL11A2 gene

21 January 2018

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Mitochondrial gene mutation is a significant predisposing factor in aminoglycoside ototoxicity.

21 January 2018

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Genes responsible for human hereditary deafness: symphony of a thousand

21 January 2018

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Autosomal dominant inherited hearing impairment caused by a missense mutation in COL11A2 (DFNA13).

21 January 2018

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Phenotype of DFNA11: a nonsyndromic hearing loss caused by a myosin VIIA mutation

21 January 2018

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Genetic screening for deafness.

21 January 2018

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MYO1F as a candidate gene for nonsyndromic deafness, DFNB15.

21 January 2018

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Presymptomatic diagnosis of nonsyndromic hearing loss by genotyping

21 January 2018

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Hearing preservation after inner ear gene therapy: the effect of vector and surgical approach.

21 January 2018

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The functional and structural outcome of inner ear gene transfer via the vestibular and cochlear fluids in mice

21 January 2018

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21 January 2018

Identifiers

DOI

10.1159/000091090

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13 August 2017

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