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

Year Number of Results
1988 1
1989 2
1992 4
1993 3
1994 4
1995 8
1996 2
1997 3
1998 4
1999 3
2000 7
2001 2
2002 1
2003 2
2004 1
2005 3
2009 5
2010 5
2011 2
2014 3
2015 1
2017 2
2018 1
2019 1
2022 3
2024 0

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Similar articles for PMID: 8589693

71 results

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Page 1
Identification of a hot spot for microdeletions in patients with X-linked deafness type 3 (DFN3) 900 kb proximal to the DFN3 gene POU3F4.
de Kok YJ, Vossenaar ER, Cremers CW, Dahl N, Laporte J, Hu LJ, Lacombe D, Fischel-Ghodsian N, Friedman RA, Parnes LS, Thorpe P, Bitner-Glindzicz M, Pander HJ, Heilbronner H, Graveline J, den Dunnen JT, Brunner HG, Ropers HH, Cremers FP. de Kok YJ, et al. Hum Mol Genet. 1996 Sep;5(9):1229-35. doi: 10.1093/hmg/5.9.1229. Hum Mol Genet. 1996. PMID: 8872461
Multiple enhancers located in a 1-Mb region upstream of POU3F4 promote expression during inner ear development and may be required for hearing.
Naranjo S, Voesenek K, de la Calle-Mustienes E, Robert-Moreno A, Kokotas H, Grigoriadou M, Economides J, Van Camp G, Hilgert N, Moreno F, Alsina B, Petersen MB, Kremer H, Gómez-Skarmeta JL. Naranjo S, et al. Hum Genet. 2010 Oct;128(4):411-9. doi: 10.1007/s00439-010-0864-x. Epub 2010 Jul 29. Hum Genet. 2010. PMID: 20668882 Free PMC article.
71 results