نتایج جستجو برای: autosomal

تعداد نتایج: 32291  

Journal: :iranian rehabilitation journal 0
reihaneh alikhani genetic research center, university of social welfare and rehabilitation sciences, tehran, iran. fatemeh ostaresh genetic research center, university of social welfare and rehabilitation sciences, tehran, iran. mojgan babanejad genetic research center, university of social welfare and rehabilitation sciences, tehran, iran. nilofar bazazzadegan genetic research center, university of social welfare and rehabilitation sciences, tehran, iran. hossein najmabadi genetic research center, university of social welfare and rehabilitation sciences, tehran, iran. kimia kahrizi genetic research center, university of social welfare and rehabilitation sciences, tehran, iran.

objectives: hearing loss (hl) is the most common sensory disorder, and affects 1 in 1000 newborns. about 50% of hl is due to genetics and 70% of them are non-syndromic with a recessive pattern of inheritance. up to now, more than 50 genes have been detected which are responsible for autosomal recessive non-syndromic hearing loss, (arnshl). in  iran, hl is one of the most common disabilities due...

Journal: :Swiss Medical Forum ‒ Schweizerisches Medizin-Forum 2009

Journal: :Advances in Chronic Kidney Disease 2017

Journal: :Canadian Medical Association Journal 2017

Journal: :Pediatric Neurology Briefs 1999

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