Imprinting mutations suggested by abnormal DNA methylation patterns in familial Angelman and Prader-Willi syndromes.

Ítems similars

• Epimutations in Prader-Willi and Angelman Syndromes: A Molecular Study of 136 Patients with an Imprinting Defect
  per: Buiting, Karin, et al.
  Publicat: (2003)
• Sporadic imprinting defects in Prader-Willi syndrome and Angelman syndrome: implications for imprint-switch models, genetic counseling, and prenatal diagnosis.
  per: Buiting, K, et al.
  Publicat: (1998)
• Clinical and molecular studies in fragile X patients with a Prader-Willi-like phenotype.
  per: Gillessen-Kaesbach, G, et al.
  Publicat: (1994)
• DNA methylation based testing of 450 patients suspected of having Prader-Willi syndrome.
  per: Gillessen-Kaesbach, G, et al.
  Publicat: (1995)
• Imprinting-mutation mechanisms in Prader-Willi syndrome.
  per: Ohta, T, et al.
  Publicat: (1999)