Different mechanisms and recurrence risks of imprinting defects in Angelman syndrome.

Lignende værker

• Epimutations in Prader-Willi and Angelman Syndromes: A Molecular Study of 136 Patients with an Imprinting Defect
  af: Buiting, Karin, et al.
  Udgivet: (2003)
• Disruption of the Bipartite Imprinting Center in a Family with Angelman Syndrome
  af: Buiting, Karin, et al.
  Udgivet: (2001)
• Imprinting mutations suggested by abnormal DNA methylation patterns in familial Angelman and Prader-Willi syndromes.
  af: Reis, A., et al.
  Udgivet: (1994)
• Sporadic imprinting defects in Prader-Willi syndrome and Angelman syndrome: implications for imprint-switch models, genetic counseling, and prenatal diagnosis.
  af: Buiting, K, et al.
  Udgivet: (1998)
• Increased prevalence of imprinting defects in patients with Angelman syndrome born to subfertile couples
  af: Ludwig, M, et al.
  Udgivet: (2005)