Prenatal correction of IGF2 to rescue the growth phenotypes in mouse models of Beckwith-Wiedemann and Silver-Russell syndromes

Lignende værker

• Genetic diagnosis of Beckwith Wiedemann syndrome and Silver-Russell syndrome
  af: Kim, Yoo-Mi, et al.
  Udgivet: (2013)
• Discrepant molecular and clinical diagnoses in Beckwith-Wiedemann and Silver-Russell syndromes
  af: Mackay, Deborah J.G., et al.
  Udgivet: (2019)
• Silver-Russell Syndrome and Beckwith-Wiedemann Syndrome: Opposite Phenotypes with Heterogeneous Molecular Etiology
  af: Õunap, Katrin
  Udgivet: (2016)
• Prenatal molecular testing for Beckwith–Wiedemann and Silver–Russell syndromes: a challenge for molecular analysis and genetic counseling
  af: Eggermann, Thomas, et al.
  Udgivet: (2016)
• Disruption of genomic neighbourhood at the imprinted IGF2-H19 locus in Beckwith–Wiedemann syndrome and Silver–Russell syndrome
  af: Nativio, Raffaella, et al.
  Udgivet: (2011)