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Results by year

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

Year Number of Results
1991 1
1992 3
1994 6
1995 8
1996 8
1997 6
1998 5
1999 7
2000 8
2001 9
2002 6
2003 10
2004 4
2005 3
2006 1
2007 3
2008 1
2009 1
2011 2
2012 1
2014 1
2015 3
2016 1
2018 1
2019 1
2020 1
2022 1
2024 0

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Similar articles for PMID: 11846731

100 results

Results by year

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Page 1
The fragile X gene and its function.
Oostra BA, Chiurazzi P. Oostra BA, et al. Clin Genet. 2001 Dec;60(6):399-408. doi: 10.1034/j.1399-0004.2001.600601.x. Clin Genet. 2001. PMID: 11846731 Review.
Fragile X syndrome at the turn of the century.
Kooy RF, Willemsen R, Oostra BA. Kooy RF, et al. Mol Med Today. 2000 May;6(5):193-8. doi: 10.1016/s1357-4310(00)01674-9. Mol Med Today. 2000. PMID: 10782066 Review.
A fragile gene.
Oostra BA, Willems PJ. Oostra BA, et al. Bioessays. 1995 Nov;17(11):941-7. doi: 10.1002/bies.950171107. Bioessays. 1995. PMID: 8526888 Review.
Fragile X syndrome.
Chakrabarti L, Davies KE. Chakrabarti L, et al. Curr Opin Neurol. 1997 Apr;10(2):142-7. doi: 10.1097/00019052-199704000-00012. Curr Opin Neurol. 1997. PMID: 9146995 Review.
100 results