The t(11;14)(q13;q32)/CCND1-IGH translocation is a recurrent secondary genetic aberration in relapsed chronic lymphocytic leukemia

Leuk Lymphoma. 2016 Nov;57(11):2672-6. doi: 10.3109/10428194.2016.1153085. Epub 2016 Feb 25.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Aged
  • Chromosomes, Human, Pair 11 / genetics*
  • Chromosomes, Human, Pair 14 / genetics*
  • Clonal Evolution / genetics
  • Gene Frequency
  • Humans
  • Leukemia, Lymphocytic, Chronic, B-Cell / genetics*
  • Leukemia, Lymphocytic, Chronic, B-Cell / pathology
  • Male
  • Middle Aged
  • Oncogene Proteins, Fusion / genetics*
  • Recurrence
  • Translocation, Genetic*

Substances

  • IGH-CCND1 fusion protein, human
  • Oncogene Proteins, Fusion