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

Eitemau Tebyg

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