Similar articles

• Mutation analysis of the methyl-CpG binding protein 2 gene (MECP2) in patients with Rett syndrome.

  Obata K, Matsuishi T, Yamashita Y, Fukuda T, Kuwajima K, Horiuchi I, Nagamitsu S, Iwanaga R, Kimura A, Omori I, Endo S, Mori K, Kondo I. Obata K, et al. J Med Genet. 2000 Aug;37(8):608-10. doi: 10.1136/jmg.37.8.608. J Med Genet. 2000. PMID: 10991688 Free PMC article. No abstract available.
• Rett syndrome and the MECP2 gene.

  Webb T, Latif F. Webb T, et al. J Med Genet. 2001 Apr;38(4):217-23. doi: 10.1136/jmg.38.4.217. J Med Genet. 2001. PMID: 11283201 Free PMC article. Review. No abstract available.
• Mutation analysis in the MECP2 gene and genetic counselling for Rett syndrome.

  Gill H, Cheadle JP, Maynard J, Fleming N, Whatley S, Cranston T, Thompson EM, Leonard H, Davis M, Christodoulou J, Skjeldal O, Hanefeld F, Kerr A, Tandy A, Ravine D, Clarke A. Gill H, et al. J Med Genet. 2003 May;40(5):380-4. doi: 10.1136/jmg.40.5.380. J Med Genet. 2003. PMID: 12746405 Free PMC article. No abstract available.
• MECP2 mutations in Swedish Rett syndrome clusters.

  Xiang F, Stenbom Y, Anvret M. Xiang F, et al. Clin Genet. 2002 May;61(5):384-5. doi: 10.1034/j.1399-0004.2002.610512.x. Clin Genet. 2002. PMID: 12081725 No abstract available.
• Rett syndrome and MeCP2: linking epigenetics and neuronal function.

  Shahbazian MD, Zoghbi HY. Shahbazian MD, et al. Am J Hum Genet. 2002 Dec;71(6):1259-72. doi: 10.1086/345360. Epub 2002 Nov 19. Am J Hum Genet. 2002. PMID: 12442230 Free PMC article. Review. No abstract available.