Clinical utility gene card for: Beckwith–Wiedemann Syndrome

Documenti analoghi

• EMQN best practice guidelines for the molecular genetic testing and reporting of chromosome 11p15 imprinting disorders: Silver–Russell and Beckwith–Wiedemann syndrome
  di: Eggermann, Katja, et al.
  Pubblicazione: (2016)
• Prenatal molecular testing for Beckwith–Wiedemann and Silver–Russell syndromes: a challenge for molecular analysis and genetic counseling
  di: Eggermann, Thomas, et al.
  Pubblicazione: (2016)
• Discrepant molecular and clinical diagnoses in Beckwith-Wiedemann and Silver-Russell syndromes
  di: Mackay, Deborah J.G., et al.
  Pubblicazione: (2019)
• Beckwith–Wiedemann syndrome
  di: Weksberg, Rosanna, et al.
  Pubblicazione: (2010)
• The two-domain hypothesis in Beckwith-Wiedemann syndrome
  di: Maher, Eamonn R., et al.
  Pubblicazione: (2000)