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

Year Number of Results
2001 2
2007 1
2008 1
2010 1
2015 1
2022 0
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6 results
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Page 1
Cowden syndrome.
Gustafson S, Zbuk KM, Scacheri C, Eng C. Gustafson S, et al. Among authors: scacheri c. Semin Oncol. 2007 Oct;34(5):428-34. doi: 10.1053/j.seminoncol.2007.07.009. Semin Oncol. 2007. PMID: 17920899 Review.
Mutations in the noncoding genome.
Scacheri CA, Scacheri PC. Scacheri CA, et al. Curr Opin Pediatr. 2015 Dec;27(6):659-64. doi: 10.1097/MOP.0000000000000283. Curr Opin Pediatr. 2015. PMID: 26382709 Free PMC article. Review.
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: scacheri c. Neurology. 2001 Jun 12;56(11):1486-95. doi: 10.1212/wnl.56.11.1486. Neurology. 2001. PMID: 11402105