Clinical utility gene card for: Beckwith–Wiedemann Syndrome

Benzer Materyaller

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