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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2004 4
2005 2
2006 1
2007 2
2008 1
2009 3
2010 1
2011 6
2012 8
2013 8
2014 9
2015 19
2016 14
2017 8
2018 10
2019 15
2020 18
2021 22
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139 results
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Page 1
ClinGen expert clinical validity curation of 164 hearing loss gene-disease pairs.
DiStefano MT, Hemphill SE, Oza AM, Siegert RK, Grant AR, Hughes MY, Cushman BJ, Azaiez H, Booth KT, Chapin A, Duzkale H, Matsunaga T, Shen J, Zhang W, Kenna M, Schimmenti LA, Tekin M, Rehm HL, Tayoun ANA, Amr SS; ClinGen Hearing Loss Clinical Domain Working Group. DiStefano MT, et al. Genet Med. 2019 Oct;21(10):2239-2247. doi: 10.1038/s41436-019-0487-0. Epub 2019 Mar 21. Genet Med. 2019. PMID: 30894701 Free PMC article.
Genetic Information and Precision Medicine in Hearing Loss.
Oh DY, Choi BY. Oh DY, et al. Among authors: choi by. Clin Exp Otorhinolaryngol. 2020 Nov;13(4):315-317. doi: 10.21053/ceo.2020.01606. Epub 2020 Nov 1. Clin Exp Otorhinolaryngol. 2020. PMID: 33176397 Free PMC article. No abstract available.
Hereditary hearing loss with thyroid abnormalities.
Choi BY, Muskett J, King KA, Zalewski CK, Shawker T, Reynolds JC, Butman JA, Brewer CC, Stewart AK, Alper SL, Griffith AJ. Choi BY, et al. Adv Otorhinolaryngol. 2011;70:43-49. doi: 10.1159/000322469. Epub 2011 Feb 24. Adv Otorhinolaryngol. 2011. PMID: 21358184 Review.
Craniometaphyseal dysplasia.
Kim YH, Roh DH, Choi BY, Oh SH. Kim YH, et al. Among authors: choi by. Acta Otolaryngol. 2005 Jul;125(7):797-800. doi: 10.1080/00016480510028474. Acta Otolaryngol. 2005. PMID: 16012045
139 results
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