Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Recurrence and GJB2[original query] |
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Exploration of molecular genetic etiology for Korean cochlear implantees with severe to profound hearing loss and its implication. Orphanet journal of rare diseases 2014 9 167. Park Joo Hyun, Kim Nayoung K D, Kim Ah Reum, Rhee Jihye, Oh Seung Ha, Koo Ja-Won, Nam Jae-Yong, Park Woong-Yang, Choi Byung Yo |
Genomic Studies in a Large Cohort of Hearing Impaired Italian Patients Revealed Several New Alleles, a Rare Case of Uniparental Disomy (UPD) and the Importance to Search for Copy Number Variations. Frontiers in genetics 2019 1 9 681. Morgan Anna, Lenarduzzi Stefania, Cappellani Stefania, Pecile Vanna, Morgutti Marcello, Orzan Eva, Ghiselli Sara, Ambrosetti Umberto, Brumat Marco, Gajendrarao Poornima, La Bianca Martina, Faletra Flavio, Grosso Enrico, Sirchia Fabio, Sensi Alberto, Graziano Claudio, Seri Marco, Gasparini Paolo, Girotto Giorg |
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 |
Low incidence of GIPC3 variants among the prelingual hearing impaired from southern India. Journal of genetics 2020 11 99 . Kalaimathi Murugesan, Subathra Mahalingam, Jeffrey Justin Margret, Selvakumari Mathiyalagan, Chandru Jayasankaran, Sharanya Narasimhan, Paridhy Vanniya S, Srisailapathy C R Srikuma |
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