(Q50488814)

14 March 2018

title

Frequency of the 35delG mutation in the connexin 26 gene in Turkish hearing-impaired patients. (English)

1 reference

14 March 2018

author name string

I Bariş

series ordinal

1

1 reference

14 March 2018

M O Kilinç

series ordinal

2

1 reference

14 March 2018

A Tolun

series ordinal

3

1 reference

14 March 2018

publication date

1 December 2001

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14 March 2018

published in

Clinical Genetics

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14 March 2018

volume

60

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14 March 2018

issue

6

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14 March 2018

page(s)

452-455

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14 March 2018

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

cites work

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.600608.X

Connexin-26 mutations in sporadic and inherited sensorineural deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.600608.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.600608.X

The prevalence and expression of inherited connexin 26 mutations associated with nonsyndromic hearing loss in the Israeli population

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.600608.X

Connexin 26 (GJB2) mutations in the Turkish population: implications for the origin and high frequency of the 35delG mutation in Caucasians

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.600608.X

High carrier frequency of the 35delG deafness mutation in European populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.600608.X

Connexin-26 mutations in sporadic non-syndromal sensorineural deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.600608.X

inferred from DOI database lookup

7 January 2021

based on heuristic

Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing loss

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.600608.X

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1034/J.1399-0004.2001.600608.X

1 reference

14 March 2018

1 reference

14 March 2018