Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Recurrence and SLC26A4[original query] |
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Use of SLC26A4 mutation testing for unilateral enlargement of the vestibular aqueduct. JAMA otolaryngology-- head & neck surgery 2013 Sep 139 (9): 907-13. Chattaraj Parna, Reimold Fabian R, Muskett Julie A, Shmukler Boris E, Chien Wade W, Madeo Anne C, Pryor Shannon P, Zalewski Christopher K, Butman John A, Brewer Carmen C, Kenna Margaret A, Alper Seth L, Griffith Andrew |
Whole Exome Sequencing Reveals Homozygous Mutations in RAI1, OTOF, and SLC26A4 Genes Associated with Nonsyndromic Hearing Loss in Altaian Families (South Siberia). PloS one 2016 11 (4): e0153841. ?hurbanov Alexander Y, Karafet Tatiana M, Morozov Igor V, Mikhalskaia Valeriia Yu, Zytsar Marina V, Bondar Alexander A, Posukh Olga |
Genetic analysis of SLC26A4 gene (pendrin) related deafness among a cohort of assortative mating families from southern India. 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 2020 May . Chandru Jayasankaran, Jeffrey Justin Margret, Pavithra Amritkumar, Vanniya S Paridhy, Devi G Nandhini, Mahalingam Subathra, Karthikeyen Natarajan Padmavathy, Srisailapathy C R Srikuma |
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