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misaki hyogo
(90 results)?
Detailed clinical features and genotype-phenotype correlation in an OTOF-related hearing loss cohort in Japan.
Hum Genet. 2022 Apr;141(3-4):865-875. doi: 10.1007/s00439-021-02351-7. Epub 2021 Sep 18.
Hum Genet. 2022.
PMID: 34536124
Free PMC article.
Correction to: Detailed clinical features and genotype-phenotype correlation in an OTOF-related hearing loss cohort in Japan.
Iwasa YI, Nishio SY, Yoshimura H, Sugaya A, Kataoka Y, Maeda Y, Kanda Y, Nagai K, Naito Y, Yamazaki H, Ikezono T, Matsuda H, Nakai M, Tona R, Sakurai Y, Motegi R, Takeda H, Kobayashi M, Kihara C, Ishino T, Morita SY, Iwasaki S, Takahashi M, Furutate S, Oka SI, Kubota T, Arai Y, Kobayashi Y, Kikuchi D, Shintani T, Ogasawara N, Honkura Y, Izumi S, Hyogo M, Ninoyu Y, Suematsu M, Nakayama J, Tsuchihashi N, Okami M, Sakata H, Yoshihashi H, Kobayashi T, Kumakawa K, Yoshida T, Esaki T, Usami SI.
Iwasa YI, et al. Among authors: hyogo m.
Hum Genet. 2022 Apr;141(3-4):993-995. doi: 10.1007/s00439-021-02392-y.
Hum Genet. 2022.
PMID: 34727261
Free PMC article.
No abstract available.
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The Prevalence and Clinical Characteristics of TECTA-Associated Autosomal Dominant Hearing Loss.
Yasukawa R, Moteki H, Nishio SY, Ishikawa K, Abe S, Honkura Y, Hyogo M, Mihashi R, Ikezono T, Shintani T, Ogasawara N, Shirai K, Yoshihashi H, Ishino T, Otsuki K, Ito T, Sugahara K, Usami SI.
Yasukawa R, et al. Among authors: hyogo m.
Genes (Basel). 2019 Sep 24;10(10):744. doi: 10.3390/genes10100744.
Genes (Basel). 2019.
PMID: 31554319
Free PMC article.
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Clinical Characteristics and In Vitro Analysis of MYO6 Variants Causing Late-Onset Progressive Hearing Loss.
Oka SI, Day TF, Nishio SY, Moteki H, Miyagawa M, Morita S, Izumi S, Ikezono T, Abe S, Nakayama J, Hyogo M, Okamoto N, Uehara N, Oshikawa C, Kitajiri SI, Usami SI.
Oka SI, et al. Among authors: hyogo m.
Genes (Basel). 2020 Mar 4;11(3):273. doi: 10.3390/genes11030273.
Genes (Basel). 2020.
PMID: 32143290
Free PMC article.
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The prevalence and clinical features of MYO7A-related hearing loss including DFNA11, DFNB2 and USH1B.
Watanabe K, Nishio SY, Usami SI; Deafness Gene Study Consortium.
Watanabe K, et al.
Sci Rep. 2024 Apr 9;14(1):8326. doi: 10.1038/s41598-024-57415-1.
Sci Rep. 2024.
PMID: 38594301
Free PMC article.
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[Congenital ossicular malformation: a study of 27 ears].
Morioka S, Sakaguchi H, Taki M, Hyogo M, Suzuki T, Hisa Y.
Morioka S, et al. Among authors: hyogo m.
Nihon Jibiinkoka Gakkai Kaiho. 2010 Oct;113(10):790-7. doi: 10.3950/jibiinkoka.113.790.
Nihon Jibiinkoka Gakkai Kaiho. 2010.
PMID: 21061566
Japanese.
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