Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Deafness and GJA1[original query] |
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Identification and genotype/phenotype correlation of mutations in a large German cohort with hearing loss. European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery 2015 Oct 272 (10): 2765-76. Beck Christopher, Pérez-Álvarez Jose Carmelo, Sigruener Alexander, Haubner Frank, Seidler Till, Aslanidis Charalampos, Strutz Jürgen, Schmitz Ge |
In search of genetic markers for nonsyndromic deafness in Africa: a study in Cameroonians and Black South Africans with the GJB6 and GJA1 candidate genes. Omics : a journal of integrative biology 2014 Jul 18 (7): 481-5. Bosch Jason, Lebeko Kamogelo, Nziale Jean Jacques Noubiap, Dandara Collet, Makubalo Nomlindo, Wonkam Ambroi |
No evidence for clinical utility in investigating the connexin genes GJB2, GJB6 and GJA1 in non-syndromic hearing loss in black Africans. South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde 2015 Jan 105 (1): 23-6. Wonkam A, Bosch J, Noubiap J J N, Lebeko K, Makubalo N, Dandara |
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