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33. 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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35. Rett syndrome: case reports and review. McIntosh RP; Simatos D; Weston HJ; Stanley TV N Z Med J; 1990 Mar; 103(886):122-5. PubMed ID: 2181354 [TBL] [Abstract][Full Text] [Related]
36. Rett syndrome: a prototypical neurodevelopmental disorder. Neul JL; Zoghbi HY Neuroscientist; 2004 Apr; 10(2):118-28. PubMed ID: 15070486 [TBL] [Abstract][Full Text] [Related]