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Results by year

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

Year Number of Results
1976 1
1978 1
1980 1
1981 1
1983 1
1987 1
1988 1
1989 1
1990 2
1991 1
1992 3
1993 3
1994 3
1995 4
1996 6
1997 7
1998 2
1999 4
2000 3
2001 3
2002 2
2003 3
2004 4
2005 2
2006 5
2007 5
2008 1
2009 3
2010 9
2011 2
2012 7
2013 2
2014 5
2015 11
2016 3
2017 5
2018 8
2019 7
2020 1
2021 5
2022 9
2024 0

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Publication date

PubMed for id: 335096

136 results

Results by year

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Page 1
Molecular study of patients with auditory neuropathy.
Carvalho GM, Ramos PZ, Castilho AM, Guimarães AC, Sartorato EL. Carvalho GM, et al. Mol Med Rep. 2016 Jul;14(1):481-90. doi: 10.3892/mmr.2016.5226. Epub 2016 May 9. Mol Med Rep. 2016. PMID: 27177047
Mutations in apoptosis-inducing factor cause X-linked recessive auditory neuropathy spectrum disorder.
Zong L, Guan J, Ealy M, Zhang Q, Wang D, Wang H, Zhao Y, Shen Z, Campbell CA, Wang F, Yang J, Sun W, Lan L, Ding D, Xie L, Qi Y, Lou X, Huang X, Shi Q, Chang S, Xiong W, Yin Z, Yu N, Zhao H, Wang J, Wang J, Salvi RJ, Petit C, Smith RJ, Wang Q. Zong L, et al. J Med Genet. 2015 Aug;52(8):523-31. doi: 10.1136/jmedgenet-2014-102961. Epub 2015 May 18. J Med Genet. 2015. PMID: 25986071 Free PMC article.
X-Linked Sensorineural Hearing Loss: A Literature Review.
Corvino V, Apisa P, Malesci R, Laria C, Auletta G, Franzé A. Corvino V, et al. Curr Genomics. 2018 Aug;19(5):327-338. doi: 10.2174/1389202919666171218163046. Curr Genomics. 2018. PMID: 30065609 Free PMC article. Review.
Connexin Mutations and Hereditary Diseases.
Qiu Y, Zheng J, Chen S, Sun Y. Qiu Y, et al. Int J Mol Sci. 2022 Apr 12;23(8):4255. doi: 10.3390/ijms23084255. Int J Mol Sci. 2022. PMID: 35457072 Free PMC article. Review.
Genetic etiology of non-syndromic hearing loss in Europe.
Del Castillo I, Morín M, Domínguez-Ruiz M, Moreno-Pelayo MA. Del Castillo I, et al. Hum Genet. 2022 Apr;141(3-4):683-696. doi: 10.1007/s00439-021-02425-6. Epub 2022 Jan 19. Hum Genet. 2022. PMID: 35044523 Review.
136 results