Human Genome Epidemiology Literature Finder
Records 1 - 8 (of 8 Records) |
Query Trace: Hearing and GJA1[original query] |
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Genetic analysis of presbycusis by arrayed primer extension. Annals of clinical and laboratory science 2008 38 (4): 352-60. Rodriguez-Paris Juan, Ballay Charles, Inserra Michelle, Stidham Katrina, Colen Tahl, Roberson Joseph, Gardner Phyllis, Schrijver Ir |
Splice variant IVS2-2A>G in the SLC26A5 (Prestin) gene in five Estonian families with hearing loss. International journal of pediatric otorhinolaryngology 2009 Jan 73 (1): 103-7. Teek Rita, Oitmaa Eneli, Kruustük Katrin, Zordania Riina, Joost Kairit, Raukas Elve, Tõnisson Neeme, Gardner Phyllis, Schrijver Iris, Kull Mart, Ounap Katr |
Genotyping with a 198 mutation arrayed primer extension array for hereditary hearing loss: assessment of its diagnostic value for medical practice. PloS one 2010 5 (7): e11804. Rodriguez-Paris Juan, Pique Lynn, Colen Tahl, Roberson Joseph, Gardner Phyllis, Schrijver Ir |
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 |
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 |
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 |
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- Page last updated:May 06, 2024
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