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

Year Number of Results
1997 1
1998 2
2000 1
2001 5
2002 3
2003 2
2004 1
2005 2
2006 7
2007 1
2009 2
2013 1
2014 1
2016 1
2019 1
2022 1
2024 0

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32 results

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Page 1
Rett syndrome: a surprising result of mutation in MECP2.
Dragich J, Houwink-Manville I, Schanen C. Dragich J, et al. Among authors: schanen c. Hum Mol Genet. 2000 Oct;9(16):2365-75. doi: 10.1093/hmg/9.16.2365. Hum Mol Genet. 2000. PMID: 11005791 Review.
Occurrence of Rett syndrome in boys.
Leonard H, Silberstein J, Falk R, Houwink-Manville I, Ellaway C, Raffaele LS, Engerström IW, Schanen C. Leonard H, et al. Among authors: schanen c. J Child Neurol. 2001 May;16(5):333-8. doi: 10.1177/088307380101600505. J Child Neurol. 2001. PMID: 11392517
[Fatal fulminant Epstein-Barr virus hepatitis].
Lazrek M, Boitrelle F, Dewilde A, Schanen C, Chopin C, Desreumaux P, Leteurtre E, Hober D. Lazrek M, et al. Among authors: schanen c. Ann Biol Clin (Paris). 2006 Mar-Apr;64(2):170-2. Ann Biol Clin (Paris). 2006. PMID: 16556529 Free article. French.
Variable phenotypic expression of a MECP2 mutation in a family.
Augenstein K, Lane JB, Horton A, Schanen C, Percy AK. Augenstein K, et al. Among authors: schanen c. J Neurodev Disord. 2009 Dec;1(4):313. doi: 10.1007/s11689-009-9034-7. J Neurodev Disord. 2009. PMID: 20151026 Free PMC article.
32 results