(Q44648339)

5 December 2017

title

GJB2 and GJB6 genes and the A1555G mitochondrial mutation are only minor causes of nonsyndromic hearing loss in the Qatari population (English)

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5 December 2017

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2

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5 December 2017

M Khalifa Alkowari

1

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5 December 2017

K Abdulhadi

3

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5 December 2017

S Dipresa

4

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5 December 2017

R Siam

5

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5 December 2017

N Najjar

6

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5 December 2017

R Badii

7

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5 December 2017

P Gasparini

8

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5 December 2017

language of work or name

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21 November 2011

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International Journal of Audiology

5 December 2017

number of pages

5

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based on heuristic

inferred from page(s)

published in

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5 December 2017

volume

51

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5 December 2017

issue

3

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5 December 2017

page(s)

181-185

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Spectrum of GJB2 mutations in a cohort of nonsyndromic hearing loss cases from the Kingdom of Saudi Arabia

5 December 2017

cites work

1 reference

https://api.crossref.org/works/10.3109%2F14992027.2011.625983

Is there any association between consanguinity and hearing loss.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14992027.2011.625983

Consanguineous marriages and their effects on common adult diseases: studies from an endogamous population

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14992027.2011.625983

Prevalence and evolutionary origins of the del(GJB6-D13S1830) mutation in the DFNB1 locus in hearing-impaired subjects: a multicenter study

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14992027.2011.625983

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%2F14992027.2011.625983

Common mutation analysis of GJB2 and GJB6 genes in affected families with autosomal recessive non-syndromic hearing loss from Iran: simultaneous detection of two common mutations (35delG/del(GJB6-D13S1830)) in the DFNB1-related deafness.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14992027.2011.625983

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14992027.2011.625983

A novel 355-357delGAG mutation and frequency of connexin-26 (GJB2) mutations in Iranian patients

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14992027.2011.625983

Forty-six genes causing nonsyndromic hearing impairment: which ones should be analyzed in DNA diagnostics?

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14992027.2011.625983

Population genetic structure of the people of Qatar

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14992027.2011.625983

Mitochondrial DNA mutations in patients with postlingual, nonsyndromic hearing impairment

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14992027.2011.625983

Progressive hearing loss, and recurrent sudden sensorineural hearing loss associated with GJB2 mutations--phenotypic spectrum and frequencies of GJB2 mutations in Austria.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14992027.2011.625983

Connexin 26 studies in patients with sensorineural hearing loss.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14992027.2011.625983

Genetic causes of nonsyndromic hearing loss in Iran in comparison with other populations

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14992027.2011.625983

Absence of deafness-associated connexin-26 (GJB2) gene mutations in the Omani population.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14992027.2011.625983

The c.IVS1+1G>A mutation in the GJB2 gene is prevalent and large deletions involving the GJB6 gene are not present in the Turkish population.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14992027.2011.625983

Prevalence of the GJB2 IVS1+1G >A mutation in Chinese hearing loss patients with monoallelic pathogenic mutation in the coding region of GJB2.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14992027.2011.625983

10.3109/14992027.2011.625983

21 January 2018

Identifiers

DOI

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5 December 2017

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