Human Genome Epidemiology Literature Finder
Records 1 - 12 (of 12 Records) |
Query Trace: GJB4[original query] |
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Analysis of gene polymorphisms associated with K ion circulation in the inner ear of patients susceptible and resistant to noise-induced hearing loss. Annals of human genetics 2009 Jul 73 (Pt 4): 411-21. Pawelczyk Malgorzata, Van Laer Lut, Fransen Erik, Rajkowska Elzbieta, Konings Annelies, Carlsson Per-Inge, Borg Erik, Van Camp Guy, Sliwinska-Kowalska Mario |
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 |
Novel and recurrent connexin 30.3 and connexin 31 mutations associated with erythrokeratoderma variabilis. Clinical and experimental dermatology 2010 12 36 (1): 88-90. Scott C A, O'Toole E A, Mohungoo M J, Messenger A, Kelsell D |
Evidence for the absence of mutations at GJB3, GJB4 and LOR in progressive symmetrical erythrokeratodermia. Clinical and experimental dermatology 2011 Jun 36 (4): 399-405. Wei S, Zhou Y, Zhang T D, Huang Z M, Zhang X B, Zhu H L, Liang B H, Lin L, Deng |
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 |
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 |
Association between mutations in the gap junction ß4 gene and nonsyndromic hearing loss: genotype-phenotype correlation patterns. Molecular medicine reports 2015 Jan 11 (1): 619-24. Li Tung-Cheng, Wang Wen-Hung, Li Chuan, Yang Jiann-J |
Diverse pattern of gap junction beta-2 and gap junction beta-4 genes mutations and lack of contribution of DFNB21, DFNB24, DFNB29, and DFNB42 loci in autosomal recessive nonsyndromic hearing loss patients in Hormozgan, Iran. Journal of research in medical sciences : the official journal of Isfahan University of Medical Sciences 2017 22 99. Laleh Masoud Akbarzadeh, Naseri Marzieh, Zonouzi Ali Akbar Poursadegh, Zonouzi Ahmad Poursadegh, Masoudi Marjan, Ahangari Najmeh, Shams Leila, Nejatizadeh Az |
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 |
Association Analysis of Candidate Gene Polymorphisms and Audiometric Measures of Noise-Induced Hearing Loss in Young Musicians. Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2020 3 41 (5): e538-e547. Bhatt Ishan Sunilkumar, Dias Raquel, Washnik Nilesh, Wang Jin, Guthrie O'neil, Skelton Michael, Lane Jeffery, Wilder Jas |
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 |
Association Analysis of Candidate Gene Polymorphisms and Tinnitus in Young Musicians. Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2021 Jul . Bhatt Ishan Sunilkumar, Dias Raquel, Torkamani A |
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- Page last updated:Apr 16, 2024
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