Structural variation in Xq28: MECP2 duplications in 1% of patients with unexplained XLMR and in 2% of male patients with severe encephalopathy

Lignende værker

• Structural variation in Xq28: MECP2 duplications in 1% of patients with unexplained XLMR and in 2% of male patients with severe encephalopathy
  af: Lugtenberg, Dorien, et al.
  Udgivet: (2009)
• ZNF674: A New Krüppel-Associated Box–Containing Zinc-Finger Gene Involved in Nonsyndromic X-Linked Mental Retardation
  af: Lugtenberg, Dorien, et al.
  Udgivet: (2006)
• Mutations in the JARID1C Gene, Which Is Involved in Transcriptional Regulation and Chromatin Remodeling, Cause X-Linked Mental Retardation
  af: Jensen, Lars Riff, et al.
  Udgivet: (2005)
• Zinc finger 81 (ZNF81) mutations associated with X-linked mental retardation
  af: Kleefstra, T, et al.
  Udgivet: (2004)
• A 3-base pair deletion, c.9711_9713del, in DMD results in intellectual disability without muscular dystrophy
  af: de Brouwer, Arjan PM, et al.
  Udgivet: (2014)