Are Specific Short Arm Variants or Heteromorphisms Over-Represented in the Chromosome 15 Deletion in Angelman or Prader-Willi Syndrome Patients?

Ítems similars

• PARENTAL ORIGIN OF CHROMOSOME 15 DELETION IN PRADER-WILLI SYNDROME
  per: Butler, Merlin G., et al.
  Publicat: (1983)
• PARENTAL ORIGIN OF CHROMOSOME 15 DELETION IN PRADER-WILLI SYNDROME
  per: Butler, MerlinG., et al.
  Publicat: (1983)
• Molecular cytogenetics of Prader-Willi and Angelman syndromes
  per: Butler, Merlin G., et al.
  Publicat: (1991)
• High Resolution Chromosome Analysis and Fluorescence In Situ Hybridization in Patients Referred for Prader-Willi or Angelman Syndrome
  per: Butler, Merlin G.
  Publicat: (1995)
• Analysis of imprinted genes in subjects with Prader-Willi syndrome and chromosome 15 abnormalities
  per: Muralidhar, Bethi, et al.
  Publicat: (1999)