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The Annals of Otology, Rhinology, and Laryngology|July 30, 2016
Detection and Confirmation of Deafness-Causing Copy Number Variations in the STRC Gene by Massively Parallel Sequencing and Comparative Genomic HybridizationHideaki Moteki, Hela Azaiez, Christina M Sloan-Heggen, et al.
Acta Oto-Laryngologica|October 22, 2024
HEARRING group genetic marker study: genetic background of CI patientsShin-Ichi Usami, Shin-Ya Nishio, Javier Gavilán, et al.
The Annals of Otology, Rhinology, and Laryngology|March 20, 2015
Novel PTPRQ mutations identified in three congenital hearing loss patients with various types of hearing lossNaoko Sakuma, Hideaki Moteki, Hela Azaiez, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|April 16, 2021
Identification of a Novel Copy Number Variation of EYA4 Causing Autosomal Dominant Non-syndromic Hearing LossTakashi Ishino, Yui Ogawa, Toru Sonoyama, et al.
Antioxidants & Redox Signaling|October 16, 2013
Ubiquinol-10 supplementation activates mitochondria functions to decelerate senescence in senescence-accelerated miceGeng Tian, Jinko Sawashita, Hiroshi Kubo, et al.
Acta Oto-Laryngologica|April 4, 2017
A nationwide multicenter study of the Cochlin tomo-protein detection test: clinical characteristics of perilymphatic fistula casesHan Matsuda, Kei Sakamoto, Tomohiro Matsumura, et al.
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