Clinical significance of copy number variations in the 11p15.5 imprinting control regions: new cases and review of the literature

Lignende værker

• Novel familial distal imprinting centre 1 (11p15.5) deletion provides further insights in imprinting regulation
  af: Kraft, Florian, et al.
  Udgivet: (2019)
• Genome-wide paternal uniparental disomy mosaicism in a woman with Beckwith–Wiedemann syndrome and ovarian steroid cell tumour
  af: Gogiel, Magdalena, et al.
  Udgivet: (2013)
• Unusual deletion of the maternal 11p15 allele in Beckwith–Wiedemann syndrome with an impact on both imprinting domains
  af: Eggermann, Thomas, et al.
  Udgivet: (2021)
• Molecular and Clinical Opposite Findings in 11p15.5 Associated Imprinting Disorders: Characterization of Basic Mechanisms to Improve Clinical Management
  af: Wesseler, Katharina, et al.
  Udgivet: (2019)
• Disruption of Imprinted Genes at Chromosome Region 11p15.5 in Paediatric Rhabdomyosarcoma
  af: Anderson, John, et al.
  Udgivet: (1999)