(Q50496575)

14 March 2018

title

Pseudodominant inheritance of DFNB1 deafness due to the common 35delG mutation. (English)

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14 March 2018

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A Pampanos

1

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14 March 2018

P Neou

2

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14 March 2018

T Iliades

3

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14 March 2018

N Apostolopoulos

4

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14 March 2018

N Voyiatzis

5

1 reference

14 March 2018

M Grigoriadou

6

1 reference

14 March 2018

L Katsichti

7

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14 March 2018

A Skevas

8

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14 March 2018

M B Petersen

9

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14 March 2018

publication date

1 March 2000

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14 March 2018

published in

Clinical Genetics

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14 March 2018

volume

57

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14 March 2018

issue

3

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14 March 2018

page(s)

232-234

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14 March 2018

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

cites work

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570311.X

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/10.1034%2FJ.1399-0004.2000.570311.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570311.X

Connexin-26 mutations in sporadic and inherited sensorineural deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570311.X

Attitudes of deaf adults toward genetic testing for hereditary deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570311.X

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/10.1034%2FJ.1399-0004.2000.570311.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570311.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570311.X

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1034/J.1399-0004.2000.570311.X

1 reference

14 March 2018

1 reference

14 March 2018