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44. Associations between MeCP2 mutations, X-chromosome inactivation, and phenotype. Hoffbuhr KC; Moses LM; Jerdonek MA; Naidu S; Hoffman EP Ment Retard Dev Disabil Res Rev; 2002; 8(2):99-105. PubMed ID: 12112735 [TBL] [Abstract][Full Text] [Related]
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