Molecular studies in the GJB2 gene (Cx26) among a deaf population from Bogotá, Colombia: Results of a screening program-Reference-Cited by-同舟云学术

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Molecular studies in the GJB2 gene (Cx26) among a deaf population from Bogotá, Colombia: Results of a screening program

Published:2009-01 Issue:1 Volume:73 Page:97-101
ISSN:0165-5876
Container-title:International Journal of Pediatric Otorhinolaryngology
language:en
Short-container-title:International Journal of Pediatric Otorhinolaryngology

Author:

Tamayo M.L.,Olarte M.,Gelvez N.,Gómez M.,Frías J.L.,Bernal J.E.,Florez S.,Medina D.

Publisher

Elsevier BV

Subject

Otorhinolaryngology,General Medicine,Pediatrics, Perinatology, and Child Health

Reference34 articles.

1. Newborn hearing screening: the great omission;Mehl;Pediatrics,1998

2. The Colorado newborn hearing screening project, 1992–1999: on the threshold of effective population-based universal newborn hearing screening;Mehl;Pediatrics,2002

3. Clinical aspects of hereditary hearing loss;Kochhar;Genet. Med.,2007

4. Genetic epidemiology of hearing impairment;Morton;Ann. N. Y. Acad. Sci.,1991

5. A non-syndromic form of neurosensory recessive deafness maps to the pericentromeric region of chromosome 13q;Guiford;Nat. Genet.,1994

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1. Molecular Mechanisms and Clinical Phenotypes of GJB2 Missense Variants;Biology;2023-03-27

2. Research Article Mutation analysis of the GJB2 gene of patients with non-syndromic hearing impairment in the Kurdish population in Sulaimani province, Iraq;Genetics and Molecular Research;2023

3. Genetic etiology of non-syndromic hearing loss in Latin America;Human Genetics;2021-10-15

4. Connexin Genes Variants Associated with Non-Syndromic Hearing Impairment: A Systematic Review of the Global Burden;Life;2020-10-28

5. Systematic Review of Pathogenic GJB2 Variants in the Latino Population;Otology & Neurotology;2020-02

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