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

Year Number of Results
1988 2
1989 1
1990 1
1992 1
1993 1
1994 1
1995 1
1996 2
1997 2
1998 2
1999 3
2000 4
2001 2
2002 5
2003 3
2004 5
2005 2
2006 3
2007 3
2008 3
2009 4
2010 4
2011 1
2012 3
2013 3
2014 5
2016 1
2017 1
2018 1
2019 2
2020 2
2021 2
2022 4
2024 3

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80 results

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Page 1
[Autism, genetics and synaptic function alterations].
Perche O, Laumonnier F, Baala L, Ardourel MY, Menuet A, Robin V, Mortaud S, Montécot-Dubourg C, Richard O, Pichon J, Briault S. Perche O, et al. Among authors: briault s. Pathol Biol (Paris). 2010 Oct;58(5):381-6. doi: 10.1016/j.patbio.2009.12.005. Epub 2010 Feb 23. Pathol Biol (Paris). 2010. PMID: 20181440 Review. French.
FMR protein: Evidence of an emerging role in retinal aging?
Ardourel M, Ranchon-Cole I, Pâris A, Felgerolle C, Acar N, Lesne F, Briault S, Perche O. Ardourel M, et al. Among authors: briault s. Exp Eye Res. 2022 Dec;225:109282. doi: 10.1016/j.exer.2022.109282. Epub 2022 Oct 17. Exp Eye Res. 2022. PMID: 36265576 Free article.
Molecular and clinical analyses with neuropsychological assessment of a case of del(10)(q26.2qter) without intellectual disability: Genomic and transcriptomic combined approach and review of the literature.
Laudier B, Epiais T, Pâris A, Menuet A, Briault S, Ozsancak C, Perche O. Laudier B, et al. Among authors: briault s. Am J Med Genet A. 2016 Jul;170(7):1806-12. doi: 10.1002/ajmg.a.37677. Epub 2016 Apr 26. Am J Med Genet A. 2016. PMID: 27113058 Review.
FG syndrome: the FGS2 locus revisited.
Perche O, Laudier B, Menuet A, Odent S, Laumonnier F, Briault S. Perche O, et al. Among authors: briault s. Am J Med Genet A. 2012 Jun;158A(6):1489-92. doi: 10.1002/ajmg.a.35322. Epub 2012 Apr 23. Am J Med Genet A. 2012. PMID: 22528511 No abstract available.
80 results