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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2007 | 1 |
2008 | 3 |
2009 | 1 |
2010 | 1 |
2024 | 0 |
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Page 1
Treatment with valproic acid ameliorates ADHD symptoms in fragile X syndrome boys.
Am J Med Genet A. 2010 Jun;152A(6):1420-7. doi: 10.1002/ajmg.a.33484.
Am J Med Genet A. 2010.
PMID: 20503316
Clinical Trial.
A missense mutation in CASK causes FG syndrome in an Italian family.
Piluso G, D'Amico F, Saccone V, Bismuto E, Rotundo IL, Di Domenico M, Aurino S, Schwartz CE, Neri G, Nigro V.
Piluso G, et al.
Am J Hum Genet. 2009 Feb;84(2):162-77. doi: 10.1016/j.ajhg.2008.12.018. Epub 2009 Feb 5.
Am J Hum Genet. 2009.
PMID: 19200522
Free PMC article.
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Epigenetic analysis reveals a euchromatic configuration in the FMR1 unmethylated full mutations.
Tabolacci E, Moscato U, Zalfa F, Bagni C, Chiurazzi P, Neri G.
Tabolacci E, et al.
Eur J Hum Genet. 2008 Dec;16(12):1487-98. doi: 10.1038/ejhg.2008.130. Epub 2008 Jul 16.
Eur J Hum Genet. 2008.
PMID: 18628788
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XLMR genes: update 2007.
Chiurazzi P, Schwartz CE, Gecz J, Neri G.
Chiurazzi P, et al.
Eur J Hum Genet. 2008 Apr;16(4):422-34. doi: 10.1038/sj.ejhg.5201994. Epub 2008 Jan 16.
Eur J Hum Genet. 2008.
PMID: 18197188
Review.
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A unique case of reversion to normal size of a maternal premutation FMR1 allele in a normal boy.
Tabolacci E, Pomponi MG, Pietrobono R, Chiurazzi P, Neri G.
Tabolacci E, et al.
Eur J Hum Genet. 2008 Feb;16(2):209-14. doi: 10.1038/sj.ejhg.5201949. Epub 2007 Oct 31.
Eur J Hum Genet. 2008.
PMID: 17971832
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