Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: GJC3[original query] |
---|
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 |
Mutations in the connexin 29 gene are not a major cause of nonsyndromic hearing impairment in India. Genetic testing and molecular biomarkers 2010 Aug 14 (4): 539-41. Ramchander Puppala Venkat, Panda Khirod Chandra, Panda Ashok Kum |
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 |
GJB4 and GJC3 variants in non-syndromic hearing impairment in Ghana. Experimental biology and medicine (Maywood, N.J.) 2020 6 245 (15): 1355-1367. Adadey Samuel M, Esoh Kevin K, Quaye Osbourne, Amedofu Geoffrey K, Awandare Gordon A, Wonkam Ambroi |
Connexin Genes Variants Associated with Non-Syndromic Hearing Impairment: A Systematic Review of the Global Burden. Life (Basel, Switzerland) 2020 10 10 (11): . Adadey Samuel Mawuli, Wonkam-Tingang Edmond, Twumasi Aboagye Elvis, Nayo-Gyan Daniel Wonder, Boatemaa Ansong Maame, Quaye Osbourne, Awandare Gordon A, Wonkam Ambroi |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
- Content source: