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Theoretical Population Biology, ISSN 0040-5809, 07/2018, Volume 122, pp. 12 - 21
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 04/2018, Volume 102, Issue 4, pp. 547 - 556
Journal Article
JOURNAL OF ANIMAL SCIENCE, ISSN 0021-8812, 09/2016, Volume 94, Issue 9, pp. 132 - 132
Conference Proceeding
Journal Article
Journal Article
Journal Article
Animal, ISSN 1751-7311, 02/2018, Volume 12, Issue 2, pp. 215 - 223
Journal Article
Journal Article
BMC MEDICAL GENETICS, ISSN 1471-2350, 08/2018, Volume 19
Background: Mutations in GJB2 gene are a major causes of deafness and their spectrum and prevalence are specific for various populations. The well-known... 
Haplotypes | Deafness | GENE MUTATION | 35DELG MUTATION | RECESSIVE DEAFNESS | CX26 GENE | GJB2 | Siberia | GENETICS & HEREDITY | ASHKENAZI JEWS | FOUNDER | ANCESTRAL HAPLOTYPE | CONGENITAL DEAFNESS | CONNEXIN-26 35DELG | c.35delG | HIGH PREVALENCE
Journal Article
Immunogenetics, ISSN 0093-7711, 11/2007, Volume 59, Issue 11, pp. 861 - 872
Journal Article