ETV6 deletion is a common additional abnormality in patients with myelodysplastic syndromes or acute myeloid leukemia and monosomy 7

Benzer Materyaller

• The Role of Dicentric Chromosome Formation and Secondary Centromere Deletion in the Evolution of Myeloid Malignancy
  Yazar:: MacKinnon, Ruth N., ve diğerleri
  Baskı/Yayın Bilgisi: (2011)
• Detailed molecular cytogenetic characterisation of the myeloid cell line U937 reveals the fate of homologous chromosomes and shows that centromere capture is a feature of genome instability
  Yazar:: MacKinnon, Ruth N., ve diğerleri
  Baskı/Yayın Bilgisi: (2020)
• CGH and SNP array using DNA extracted from fixed cytogenetic preparations and long-term refrigerated bone marrow specimens
  Yazar:: MacKinnon, Ruth N, ve diğerleri
  Baskı/Yayın Bilgisi: (2012)
• Genome organization and the role of centromeres in evolution of the erythroleukaemia cell line HEL
  Yazar:: MacKinnon, Ruth N., ve diğerleri
  Baskı/Yayın Bilgisi: (2013)
• Corticosteroid-resistant Sweet syndrome in the setting of acute myeloid leukemia with monosomy 7 and 5q deletion
  Yazar:: Roche, Fritzlaine C., ve diğerleri
  Baskı/Yayın Bilgisi: (2020)