(Q44875844)

7 December 2017

title

Relation between choice of partner and high frequency of connexin-26 deafness (English)

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7 December 2017

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W E Nance

1

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7 December 2017

X Z Liu

series ordinal

2

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7 December 2017

A Pandya

series ordinal

3

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7 December 2017

language of work or name

English

0 references

publication date

1 August 2000

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7 December 2017

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7 December 2017

volume

356

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7 December 2017

issue

9228

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7 December 2017

page(s)

500-501

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Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

7 December 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2800%2902565-4

7 January 2021

Connexin-26 mutations in sporadic and inherited sensorineural deafness

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2800%2902565-4

7 January 2021

Connexin 26 gene mutation and autosomal recessive deafness

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2800%2902565-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2800%2902565-4

7 January 2021

The Correlation between Relatives on the Supposition of Mendelian Inheritance

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2800%2902565-4

7 January 2021

Carrier rates in the midwestern United States for GJB2 mutations causing inherited deafness.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2800%2902565-4

7 January 2021

Three novel connexin26 gene mutations in autosomal recessive non-syndromic deafness

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2800%2902565-4

7 January 2021

10.1016/S0140-6736(00)02565-4

Identifiers

DOI

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7 December 2017

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