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

Year Number of Results
1993 1
1996 1
2000 1
2001 2
2002 2
2003 3
2009 1
2010 1
2011 1
2022 0
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11 results
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Page 1
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. Neurology. 2001 Jun 12;56(11):1486-95. doi: 10.1212/wnl.56.11.1486. Neurology. 2001. PMID: 11402105
11 results