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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Dec 9, 2024. (Total: 234232Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Keratitis and GJB2[original query]
Auditory perception and speech discrimination after cochlear implantation in patients with connexin 26 (GJB2) gene-related deafness.
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2004 Nov 25 (6): 930-4.
Sinnathuray Arasa Raj, Toner Joseph G, Geddis Andrea, Clarke-Lyttle Joanne, Patterson Christopher C, Hughes Anne
Expanding the phenotypic spectrum of Cx26 disorders: Bart-Pumphrey syndrome is caused by a novel missense mutation in GJB2.
The Journal of investigative dermatology 2004 Nov 123 (5): 856-63.
Richard Gabriele, Brown Nkecha, Ishida-Yamamoto Akemi, Krol Alfo
First-Line Molecular Genetic Evaluation of Autosomal Recessive Non-Syndromic Hearing Loss.
Turkish archives of otorhinolaryngology 2019 10 57 (3): 140-148.
Özy?lmaz Berk, Mercan Gül Caner, K?rb?y?k Özgür, Özdemir Taha Re?id, Özkara Samira, Kaya Özge Özer, Kutbay Ya?ar Bekir, Erdo?an Kadri Murat, Güvenç Merve Saka, Koç Alt
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