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ORIGINAL ARTICLE
Detection of 35delG, 167delT mutations in the connexin 26 gene among Egyptian patients with nonsyndromic sensorineural hearing loss El Barbary Nehal E, El Belbesy Mervat F, Asal Samir I, Kholeif Soha F
Year : 2015 | Volume: 31 | Issue Number: 1 | Page: 42-46
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