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Meins M., Lehmann J., Gerresheim F., Herchenbach J., Hagedorn M., Hameister K., and Epplen J.T., 2005. Submicroscopic duplication in Xq28 causes increased expression of the MECP2 gene in a boy with severe mental retardation and features of Rett syndrome. J. Med. Genet. 42: el2.

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