(Q40510994)

English

Audiological profile of the prevalent genetic form of childhood sensorineural hearing loss due to GJB2 mutations in northern Greece

scientific article published on 30 September 2003

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Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

21 September 2017

Audiological profile of the prevalent genetic form of childhood sensorineural hearing loss due to GJB2 mutations in northern Greece (English)

1 reference

Europe PubMed Central

PubMed publication ID

21 September 2017

1 reference

based on heuristic

inferred from title

sensorineural hearing loss

1 reference

based on heuristic

inferred from title

author name string

V Iliadou

1

1 reference

Europe PubMed Central

PubMed publication ID

21 September 2017

N Eleftheriades

2

1 reference

Europe PubMed Central

PubMed publication ID

21 September 2017

A S Metaxas

3

1 reference

Europe PubMed Central

PubMed publication ID

21 September 2017

A Skevas

4

1 reference

Europe PubMed Central

PubMed publication ID

21 September 2017

T Kiratzidis

5

1 reference

Europe PubMed Central

PubMed publication ID

21 September 2017

A Pampanos

6

1 reference

Europe PubMed Central

PubMed publication ID

21 September 2017

N Voyiatzis

7

1 reference

Europe PubMed Central

PubMed publication ID

21 September 2017

M Grigoriadou

8

1 reference

Europe PubMed Central

PubMed publication ID

21 September 2017

M B Petersen

9

1 reference

Europe PubMed Central

PubMed publication ID

21 September 2017

T Iliades

10

1 reference

Europe PubMed Central

PubMed publication ID

21 September 2017

publication date

30 September 2003

1 reference

Europe PubMed Central

PubMed publication ID

21 September 2017

European Archives of Oto-Rhino-Laryngology

1 reference

Europe PubMed Central

PubMed publication ID

21 September 2017

261

1 reference

Europe PubMed Central

PubMed publication ID

21 September 2017

5

1 reference

Europe PubMed Central

PubMed publication ID

21 September 2017

259-261

1 reference

Europe PubMed Central

PubMed publication ID

21 September 2017

https://scigraph.springernature.com/pub.10.1007/s00405-003-0679-7

0 references

Prelingual nonsyndromic hearing loss in Greece. Molecular and clinical findings.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15138772

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High frequency hearing loss correlated with mutations in the GJB2 gene.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15138772

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/15138772

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular genetics of hearing impairment due to mutations in gap junction genes encoding beta connexins

1 reference

https://pubmed.ncbi.nlm.nih.gov/15138772

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Connexin-26 mutations in sporadic and inherited sensorineural deafness

1 reference

https://pubmed.ncbi.nlm.nih.gov/15138772

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prevalence of GJB2 mutations in prelingual deafness in the Greek population.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15138772

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cx26 deafness: mutation analysis and clinical variability

1 reference

https://pubmed.ncbi.nlm.nih.gov/15138772

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical phenotype and mutations in connexin 26 (DFNB1/GJB2), the most common cause of childhood hearing loss

1 reference

https://pubmed.ncbi.nlm.nih.gov/15138772

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/15138772

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The epidemiology of childhood hearing impairment: factor relevant to planning of services

1 reference

https://pubmed.ncbi.nlm.nih.gov/15138772

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High prevalence in the Greek population of the 35delG mutation in the connexin 26 gene causing prelingual deafness

1 reference

https://pubmed.ncbi.nlm.nih.gov/15138772

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Connexin 26 studies in patients with sensorineural hearing loss.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15138772

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/15138772

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital non-syndromal sensorineural hearing impairment due to connexin 26 gene mutations--molecular and audiological findings.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15138772

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00405-003-0679-7

1 reference

Europe PubMed Central

PubMed publication ID

21 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

21 September 2017

ResearchGate publication ID

0 references

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