Translocation t(2;7)(p11.2;q21.2): a rare genetic aberration associated with B-cell lymphoproliferative disorders of marginal-zone origin

Cancer Genet. 2014 Jun;207(6):281-3. doi: 10.1016/j.cancergen.2014.06.026. Epub 2014 Jun 25.
No abstract available

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Aged, 80 and over
  • Chromosomes, Human, Pair 2*
  • Chromosomes, Human, Pair 7*
  • Female
  • Humans
  • Lymphoma, B-Cell, Marginal Zone / genetics*
  • Lymphoma, B-Cell, Marginal Zone / pathology
  • Male
  • Middle Aged
  • Translocation, Genetic*