Minimal definition of the imprinting center and fixation of chromosome 15q11-q13 epigenotype by imprinting mutations.

Ítems similars

• Imprinting-mutation mechanisms in Prader-Willi syndrome.
  per: Ohta, T, et al.
  Publicat: (1999)
• Identification of a silencing element in the human 15q11-q13 imprinting center by using transgenic Drosophila
  per: Lyko, Frank, et al.
  Publicat: (1998)
• Molecular mechanism of angelman syndrome in two large families involves an imprinting mutation.
  per: Ohta, T, et al.
  Publicat: (1999)
• Disruption of the Bipartite Imprinting Center in a Family with Angelman Syndrome
  per: Buiting, Karin, et al.
  Publicat: (2001)
• Evaluation of potential models for imprinted and nonimprinted components of human chromosome 15q11-q13 syndromes by fine-structure homology mapping in the mouse.
  per: Nicholls, R D, et al.
  Publicat: (1993)