Genetic heterogeneity of congenital hearing impairment in Algerians from the Ghardaïa province-Reference-Cited by-同舟云学术

Genetic heterogeneity of congenital hearing impairment in Algerians from the Ghardaïa province

Published:2018-09 Issue: Volume:112 Page:1-5
ISSN:0165-5876
Container-title:International Journal of Pediatric Otorhinolaryngology
language:en
Short-container-title:International Journal of Pediatric Otorhinolaryngology

Author:

Talbi Sonia,Bonnet Crystel,Riahi Zied,Boudjenah Farid^ORCID,Dahmani Malika,Hardelin Jean-Pierre,Wong Jun Tai Fabienne,Louha Malek,Ammar-Khodja Fatima,Petit Christine

Funder

Algerian government

LabEx Lifesenses

Fondation BNP Paribas

Fondation Raymonde & Guy Strittmatter

Publisher

Elsevier BV

Subject

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

Reference35 articles.

1. Genomic ancestry of North Africans supports back-to-Africa migrations;Henn;PLoS Genet.,2012

2. Analysis of Y-chromosomal SNP haplogroups and STR haplotypes in an Algerian population sample;Robino;Int. J. Leg. Med.,2008

3. Ethnic simplification: moors, Arabs and Berbers (18th-20th centuries);Pouillon;Cah. d’Études Afr.,1993

4. Contested identities: Berbers, ‘Berberism’ and the state in North Africa;Maddy-Weitzman;J. North Afr. Stud.,2001

5. Genetic epidemiological studies of early-onset deafness in the U.S. school-age population;Marazita;Am. J. Med. Genet.,1993

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