(Q43075593)

English

Autosomal recessive non-syndromic hearing loss in the Lebanese population: prevalence of the 30delG mutation and report of two novel mutations in the connexin 26 (GJB2) gene.

scientific article published in October 2001

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scholarly article

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11584050%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

Autosomal recessive non-syndromic hearing loss in the Lebanese population: prevalence of the 30delG mutation and report of two novel mutations in the connexin 26 (GJB2) gene (English)

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11584050%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

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1 reference

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inferred from title

Christine Petit

8

1 reference

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11584050%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

Valerie Delague

3

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11 November 2019

author name string

M Mustapha

1

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11 November 2019

N Salem

2

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11 November 2019

E Chouery

4

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11 November 2019

M Ghassibeh

5

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11 November 2019

M Rai

6

1 reference

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11 November 2019

J Loiselet

7

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11 November 2019

A Mégarbané

9

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11 November 2019

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1 October 2001

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11 November 2019

Journal of Medical Genetics

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11 November 2019

38

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11 November 2019

10

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11 November 2019

E36

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11 November 2019

Identifiers

10.1136/JMG.38.10.E36

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11584050%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

PMC publication ID

1 reference

Europe PubMed Central

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11 November 2019

PubMed publication ID

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11 November 2019

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