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

Year Number of Results
1989 2
1990 7
1991 3
1992 16
1993 8
1994 4
1995 6
1996 3
1997 10
1998 12
1999 6
2000 5
2001 11
2002 11
2003 17
2004 17
2005 22
2006 15
2007 15
2008 13
2009 7
2010 3
2011 8
2012 10
2013 9
2014 5
2015 1
2024 0

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240 results

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Page 1
Epigenetics and human disease.
Jiang YH, Bressler J, Beaudet AL. Jiang YH, et al. Annu Rev Genomics Hum Genet. 2004;5:479-510. doi: 10.1146/annurev.genom.5.061903.180014. Annu Rev Genomics Hum Genet. 2004. PMID: 15485357 Review.
MeCP2 dysfunction in humans and mice.
Zoghbi HY. Zoghbi HY. J Child Neurol. 2005 Sep;20(9):736-40. doi: 10.1177/08830738050200090701. J Child Neurol. 2005. PMID: 16225828 Review.
Transcription, translation and fragile X syndrome.
Garber K, Smith KT, Reines D, Warren ST. Garber K, et al. Curr Opin Genet Dev. 2006 Jun;16(3):270-5. doi: 10.1016/j.gde.2006.04.010. Epub 2006 May 2. Curr Opin Genet Dev. 2006. PMID: 16647847 Review.
Gene therapy for inborn errors of liver metabolism.
Brunetti-Pierri N, Lee B. Brunetti-Pierri N, et al. Mol Genet Metab. 2005 Sep-Oct;86(1-2):13-24. doi: 10.1016/j.ymgme.2005.07.015. Mol Genet Metab. 2005. PMID: 16154372 Review.
240 results