(Q50495557)

14 March 2018

title

Molecular genetics applied to clinical practice: the Cx26 hearing impairment. (English)

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14 March 2018

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E Orzan

1

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14 March 2018

R Polli

2

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14 March 2018

M Martella

3

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14 March 2018

C Vinanzi

4

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14 March 2018

M Leonardi

5

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14 March 2018

A Murgia

6

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14 March 2018

publication date

1 October 1999

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14 March 2018

International Journal of Audiology

number of pages

5

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based on heuristic

inferred from page(s)

published in

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14 March 2018

volume

33

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14 March 2018

issue

5

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14 March 2018

page(s)

291-295

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14 March 2018

Clinical studies of families with hearing loss attributable to mutations in the connexin 26 gene (GJB2/DFNB1)

cites work

1 reference

https://api.crossref.org/works/10.3109%2F03005369909090112

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F03005369909090112

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F03005369909090112

Connexin-26 mutations in sporadic and inherited sensorineural deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F03005369909090112

Epidemiology of permanent childhood hearing impairment in Trent Region, 1985-1993.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F03005369909090112

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F03005369909090112

10.3109/03005369909090112

21 January 2018

Identifiers

DOI

1 reference

14 March 2018

1 reference

14 March 2018