Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Hearing Loss and GJC3[original query] |
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Prospective variants screening of connexin genes in children with hearing impairment: genotype/phenotype correlation. Human genetics 2010 Sep 128 (3): 303-13. Yang Jiann-Jou, Wang Wen-Hung, Lin Yen-Chun, Weng Hsu-Huei, Yang Jen-Tsung, Hwang Chung-Feng, Wu Che-Min, Li Shuan-Y |
Digenic inheritance in autosomal recessive non-syndromic hearing loss cases carrying GJB2 heterozygote mutations: assessment of GJB4, GJA1, and GJC3. International journal of pediatric otorhinolaryngology 2013 Feb 77 (2): 189-93. Kooshavar Daniz, Tabatabaiefar Mohammad Amin, Farrokhi Effat, Abolhasani Marziye, Noori-Daloii Mohammad-Reza, Hashemzadeh-Chaleshtori Morte |
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