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Nature Communications|March 14, 2020
Digenic inheritance of mutations in EPHA2 and SLC26A4 in Pendred syndromeMengnan Li, Shin-Ya Nishio, Chie Naruse, et al.
American Journal of Medical Genetics. Part A|October 3, 2022
Comprehensive genetic screening for vascular Ehlers-Danlos syndrome through an amplification-based next-generation sequencing systemTomomi Yamaguchi, Shujiro Hayashi, Daisuke Hayashi, et al.
Acta Oto-Laryngologica|April 4, 2017
Epidemiological survey of acute low-tone sensorineural hearing lossHiroaki Sato, Shigeru Kuwashima, Shin-Ya Nishio, et al.
Human Genetics|May 9, 2020
A comparative analysis of genetic hearing loss phenotypes in European/American and Japanese populationsW Daniel Walls, Hideaki Moteki, Taylor R Thomas, et al.
Acta Oto-Laryngologica|April 11, 2017
Nationwide epidemiological survey of idiopathic sudden sensorineural hearing loss in JapanRyosuke Kitoh, Shin-Ya Nishio, Kaoru Ogawa, et al.
Acta Oto-Laryngologica|April 1, 2017
The effect of initial treatment on hearing prognosis in idiopathic sudden sensorineural hearing loss: a nationwide survey in JapanMasahiro Okada, Naohito Hato, Shin-Ya Nishio, et al.
Scientific Reports|August 21, 2019
Comprehensive analysis of syndromic hearing loss patients in JapanMichie Ideura, Shin-Ya Nishio, Hideaki Moteki, et al.
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