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

Year Number of Results
1997 1
1998 1
2001 1
2004 2
2005 2
2010 1
2011 1
2016 1
2017 2
2018 1
2022 0
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12 results
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Sirianni NM, Yuan H, Rice JE, Kaufman RS, Deng J, Fulton C, Wangh LJ. Sirianni NM, et al. Genome. 2016 Nov;59(11):1049-1061. doi: 10.1139/gen-2016-0026. Epub 2016 Aug 30. Genome. 2016. PMID: 27809602 Free article.
MeCP2 mutations in children with and without the phenotype of Rett syndrome.
Hoffbuhr K, Devaney JM, LaFleur B, Sirianni N, Scacheri C, Giron J, Schuette J, Innis J, Marino M, Philippart M, Narayanan V, Umansky R, Kronn D, Hoffman EP, Naidu S. Hoffbuhr K, et al. Among authors: sirianni n. Neurology. 2001 Jun 12;56(11):1486-95. doi: 10.1212/wnl.56.11.1486. Neurology. 2001. PMID: 11402105
12 results