(Q38320851)

English

Determination of the carrier frequency of the common GJB2 (connexin-26) 35delG mutation in the Belgian population using an easy and reliable screening method

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

2 September 2017

Determination of the carrier frequency of the common GJB2 (connexin-26) 35delG mutation in the Belgian population using an easy and reliable screening method (English)

1 reference

Europe PubMed Central

PubMed publication ID

2 September 2017

4

1 reference

Europe PubMed Central

PubMed publication ID

2 September 2017

author name string

K Storm

1

1 reference

Europe PubMed Central

PubMed publication ID

2 September 2017

S Willocx

2

1 reference

Europe PubMed Central

PubMed publication ID

2 September 2017

K Flothmann

3

1 reference

Europe PubMed Central

PubMed publication ID

2 September 2017

publication date

1 January 1999

1 reference

Europe PubMed Central

PubMed publication ID

2 September 2017

1 reference

Europe PubMed Central

PubMed publication ID

2 September 2017

14

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Europe PubMed Central

PubMed publication ID

2 September 2017

3

1 reference

Europe PubMed Central

PubMed publication ID

2 September 2017

263-266

1 reference

Europe PubMed Central

PubMed publication ID

2 September 2017

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

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-1004%281999%2914%3A3%3C263%3A%3AAID-HUMU10%3E3.0.CO%3B2-X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-1004%281999%2914%3A3%3C263%3A%3AAID-HUMU10%3E3.0.CO%3B2-X

21 January 2018

Connexin-26 mutations in sporadic and inherited sensorineural deafness

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-1004%281999%2914%3A3%3C263%3A%3AAID-HUMU10%3E3.0.CO%3B2-X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-1004%281999%2914%3A3%3C263%3A%3AAID-HUMU10%3E3.0.CO%3B2-X

21 January 2018

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-1004%281999%2914%3A3%3C263%3A%3AAID-HUMU10%3E3.0.CO%3B2-X

21 January 2018

A Moroccan family with autosomal recessive sensorineural hearing loss caused by a mutation in the gap junction protein gene connexin 26 (GJB2).

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-1004%281999%2914%3A3%3C263%3A%3AAID-HUMU10%3E3.0.CO%3B2-X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-1004%281999%2914%3A3%3C263%3A%3AAID-HUMU10%3E3.0.CO%3B2-X

21 January 2018

Genetic epidemiology of hearing impairment

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-1004%281999%2914%3A3%3C263%3A%3AAID-HUMU10%3E3.0.CO%3B2-X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-1004%281999%2914%3A3%3C263%3A%3AAID-HUMU10%3E3.0.CO%3B2-X

21 January 2018

Connexin-26 mutations in sporadic non-syndromal sensorineural deafness

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-1004%281999%2914%3A3%3C263%3A%3AAID-HUMU10%3E3.0.CO%3B2-X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-1004%281999%2914%3A3%3C263%3A%3AAID-HUMU10%3E3.0.CO%3B2-X

21 January 2018

Identifiers

10.1002/(SICI)1098-1004(1999)14:3<263::AID-HUMU10>3.0.CO;2-X

1 reference

Europe PubMed Central

PubMed publication ID

2 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 September 2017

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