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

Year Number of Results
1905 1
1959 1
1962 2
1963 1
1976 1
1991 1
1993 1
1995 1
1996 1
1997 1
1998 3
1999 2
2000 3
2001 5
2002 2
2003 4
2004 5
2005 3
2006 6
2007 8
2008 5
2009 2
2010 1
2011 2
2016 1
2018 3
2019 1
2020 1
2021 1
2024 0

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Similar articles for PMID: 10220138

63 results

Results by year

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Page 1
Mitochondrial deafness mutations reviewed.
Fischel-Ghodsian N. Fischel-Ghodsian N. Hum Mutat. 1999;13(4):261-70. doi: 10.1002/(SICI)1098-1004(1999)13:4<261::AID-HUMU1>3.0.CO;2-W. Hum Mutat. 1999. PMID: 10220138 Review.
Mitochondrial deafness.
Kokotas H, Petersen MB, Willems PJ. Kokotas H, et al. Clin Genet. 2007 May;71(5):379-91. doi: 10.1111/j.1399-0004.2007.00800.x. Clin Genet. 2007. PMID: 17489842 Review.
Mitochondrial deafness.
Fischel-Ghodsian N. Fischel-Ghodsian N. Ear Hear. 2003 Aug;24(4):303-13. doi: 10.1097/01.AUD.0000079802.82344.B5. Ear Hear. 2003. PMID: 12923421 Review.
Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA mutation in 16 Chinese families: implication for early detection and prevention of deafness.
Dai P, Liu X, Han D, Qian Y, Huang D, Yuan H, Li W, Yu F, Zhang R, Lin H, He Y, Yu Y, Sun Q, Qin H, Li R, Zhang X, Kang D, Cao J, Young WY, Guan MX. Dai P, et al. Biochem Biophys Res Commun. 2006 Feb 3;340(1):194-9. doi: 10.1016/j.bbrc.2005.11.156. Biochem Biophys Res Commun. 2006. PMID: 16375862 Clinical Trial.
63 results