Clinical utility gene card for: Prader-Willi Syndrome

Ítems similars

• Clinical utility gene card for: Angelman Syndrome
  per: Buiting, Karin, et al.
  Publicat: (2015)
• Epimutations in Prader-Willi and Angelman Syndromes: A Molecular Study of 136 Patients with an Imprinting Defect
  per: Buiting, Karin, et al.
  Publicat: (2003)
• Prader–Willi syndrome
  per: Cassidy, Suzanne B, et al.
  Publicat: (2009)
• Clinical and molecular studies in fragile X patients with a Prader-Willi-like phenotype.
  per: Gillessen-Kaesbach, G, et al.
  Publicat: (1994)
• A paternal deletion of MKRN3, MAGEL2 and NDN does not result in Prader–Willi syndrome
  per: Kanber, Deniz, et al.
  Publicat: (2009)