Prader-Willi syndrome and a deletion/duplication within the 15q11-q13 region

Antzeko izenburuak

• Prader-Willi, Angelman, and 15q11-q13 duplication syndromes
  nork: Kalsner, Louisa, et al.
  Argitaratua: (2015)
• An Interstitial 15q11-q14 Deletion: Expanded Prader-Willi Syndrome Phenotype
  nork: Butler, Merlin G., et al.
  Argitaratua: (2010)
• Prader-Willi syndrome and atypical submicroscopic 15q11-q13 deletions with or without imprinting defects
  nork: Hassan, Maaz, et al.
  Argitaratua: (2016)
• Microarray analysis of gene/transcript expression in Prader-Willi syndrome: deletion versus UPD
  nork: Bittel, D, et al.
  Argitaratua: (2003)
• Inter- and intrachromosomal rearrangements are both involved in the origin of 15q11-q13 deletions in Prader-Willi syndrome.
  nork: Carrozzo, R, et al.
  Argitaratua: (1997)