Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: Syndrome 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 |
Connexin43 mutation causes heterogeneous gap junction loss and sudden infant death. Circulation 2012 Jan 125 (3): 474-81. Van Norstrand David W, Asimaki Angeliki, Rubinos Clio, Dolmatova Elena, Srinivas Miduturu, Tester David J, Saffitz Jeffrey E, Duffy Heather S, Ackerman Michael |
A known mutation in GJB6 in a large Chinese family with hidrotic ectodermal dysplasia. Journal of the European Academy of Dermatology and Venereology : JEADV 2016 May . Yang R, Hu Zl, Kong Qt, Li Ww, Zhang Ll, Du X, Huang Sy, Xia Xy, Sang |
GJA1 gene variations in sudden unexplained nocturnal death syndrome in the Chinese Han population. Forensic science international 2016 Dec 270 178-182. Wu Qiuping, Wu Yeda, Zhang Liyong, Zheng Jinxiang, Tang Shuangbo, Cheng Jiandi |
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