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Results by year

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

Year Number of Results
2004 2
2005 1
2009 1
2010 1
2011 1
2012 1
2013 3
2014 1
2015 1
2016 1
2020 1
2023 0

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PubMed for id: 453237

11 results

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Page 1
Functional null mutations of MSRB3 encoding methionine sulfoxide reductase are associated with human deafness DFNB74.
Ahmed ZM, Yousaf R, Lee BC, Khan SN, Lee S, Lee K, Husnain T, Rehman AU, Bonneux S, Ansar M, Ahmad W, Leal SM, Gladyshev VN, Belyantseva IA, Van Camp G, Riazuddin S, Friedman TB, Riazuddin S. Ahmed ZM, et al. Am J Hum Genet. 2011 Jan 7;88(1):19-29. doi: 10.1016/j.ajhg.2010.11.010. Epub 2010 Dec 23. Am J Hum Genet. 2011. PMID: 21185009 Free PMC article.
[Analysis of MYO15A variation in children with DFNB3].
Ren SM, Wu QH, Jiao ZH, Chen YB, Chen C, Kong XD, Qin ZB. Ren SM, et al. Zhonghua Er Ke Za Zhi. 2020 Oct 2;58(10):818-823. doi: 10.3760/cma.j.cn112140-20200220-00115. Zhonghua Er Ke Za Zhi. 2020. PMID: 32987461 Chinese.
Significance of unilateral enlarged vestibular aqueduct.
Greinwald J, DeAlarcon A, Cohen A, Uwiera T, Zhang K, Benton C, Halstead M, Meinzen-Derr J. Greinwald J, et al. Laryngoscope. 2013 Jun;123(6):1537-46. doi: 10.1002/lary.23889. Epub 2013 Feb 9. Laryngoscope. 2013. PMID: 23401162
11 results