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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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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.
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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.
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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
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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.
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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.
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[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.
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