Submicroscopic duplication in Xq28 causes increased expression of the MECP2 gene in a boy with severe mental retardation and features of Rett syndrome

Lignende værker

• Xq28 duplications including MECP2 in five females: Expanding the phenotype to severe mental retardation
  af: Bijlsma, E.K., et al.
  Udgivet: (2012)
• Characterizing the Phenotypic Effect of Xq28 Duplication Size in MECP2 Duplication Syndrome
  af: Peters, S.U., et al.
  Udgivet: (2019)
• Rett Syndrome in Males: The Different Clinical Course in Two Brothers with the Same Microduplication MECP2 Xq28
  af: Pitzianti, Maria Bernarda, et al.
  Udgivet: (2019)
• Overlapping submicroscopic deletions in Xq28 in two unrelated boys with developmental disorders: identification of a gene near FRAXE.
  af: Gedeon, A K, et al.
  Udgivet: (1995)
• Xq28 and lupus: IRAK1 or MECP2?
  af: Sawalha, Amr H.
  Udgivet: (2009)