High Resolution Chromosome Analysis and Fluorescence In Situ Hybridization in Patients Referred for Prader-Willi or Angelman Syndrome

Gelijkaardige items

• Comparison of high resolution cytogenetics, fluorescence in situ hybridisation, and DNA studies to validate the diagnosis of Prader-Willi and Angelman's syndromes.
  door: Smith, A, et al.
  Gepubliceerd in: (1995)
• Molecular cytogenetics of Prader-Willi and Angelman syndromes
  door: Butler, Merlin G., et al.
  Gepubliceerd in: (1991)
• Methylation PCR Analysis of Prader-Willi Syndrome, Angelman Syndrome, and Control Subjects
  door: Muralidhar, Bethi, et al.
  Gepubliceerd in: (1998)
• Are Specific Short Arm Variants or Heteromorphisms Over-Represented in the Chromosome 15 Deletion in Angelman or Prader-Willi Syndrome Patients?
  door: Butler, Merlin G.
  Gepubliceerd in: (1994)
• Prader-Willi syndrome: Methylation study or fluorescence in situ hybridization first?
  door: Hamzi, Khalil, et al.
  Gepubliceerd in: (2010)