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

Year Number of Results
1982 23
1983 36
1984 51
1985 51
1986 82
1987 52
1988 79
1989 46
1990 67
1991 122
1992 139
1993 118
1994 137
1995 98
1996 144
1997 102
1998 97
1999 113
2000 102
2001 90
2002 92
2003 83
2004 86
2005 114
2006 81
2007 104
2008 120
2009 102
2010 111
2011 135
2012 126
2013 138
2014 138
2015 132
2016 131
2017 108
2018 90
2019 96
2020 119
2021 130
2022 130
2023 92
2024 55

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3,974 results

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Page 1
Fragile X Syndrome: From Molecular Aspect to Clinical Treatment.
Protic DD, Aishworiya R, Salcedo-Arellano MJ, Tang SJ, Milisavljevic J, Mitrovic F, Hagerman RJ, Budimirovic DB. Protic DD, et al. Int J Mol Sci. 2022 Feb 9;23(4):1935. doi: 10.3390/ijms23041935. Int J Mol Sci. 2022. PMID: 35216055 Free PMC article. Review.
Rare FMR1 gene mutations causing fragile X syndrome: A review.
Sitzmann AF, Hagelstrom RT, Tassone F, Hagerman RJ, Butler MG. Sitzmann AF, et al. Am J Med Genet A. 2018 Jan;176(1):11-18. doi: 10.1002/ajmg.a.38504. Epub 2017 Nov 27. Am J Med Genet A. 2018. PMID: 29178241 Free PMC article. Review.
Autism and fragile X syndrome.
Yu TW, Berry-Kravis E. Yu TW, et al. Semin Neurol. 2014 Jul;34(3):258-65. doi: 10.1055/s-0034-1386764. Epub 2014 Sep 5. Semin Neurol. 2014. PMID: 25192504 Review.
Developmental studies in fragile X syndrome.
Razak KA, Dominick KC, Erickson CA. Razak KA, et al. J Neurodev Disord. 2020 May 2;12(1):13. doi: 10.1186/s11689-020-09310-9. J Neurodev Disord. 2020. PMID: 32359368 Free PMC article. Review.
The fragile X syndrome.
Jacobs PA. Jacobs PA. J Med Genet. 1991 Dec;28(12):809-10. doi: 10.1136/jmg.28.12.809. J Med Genet. 1991. PMID: 1757953 Free PMC article. No abstract available.
[Fragile X syndrome].
Glóver-López G, Guillén-Navarro E. Glóver-López G, et al. Rev Neurol. 2006 Jan 7;42 Suppl 1:S51-4. Rev Neurol. 2006. PMID: 16506133 Free article. Review. Spanish.
3,974 results