A complex 1;19;11 translocation involving the MLL gene in a patient with congenital acute monoblastic leukemia identified by molecular and cytogenetic techniques

Ann Hematol. 2009 Aug;88(8):795-7. doi: 10.1007/s00277-008-0656-8. Epub 2008 Dec 24.
No abstract available

Publication types

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

MeSH terms

  • Chromosomes, Human, Pair 1
  • Chromosomes, Human, Pair 11
  • Chromosomes, Human, Pair 19
  • Cyanosis
  • Fatal Outcome
  • Female
  • Histone-Lysine N-Methyltransferase
  • Humans
  • Infant, Newborn
  • Leukemia, Monocytic, Acute / congenital
  • Leukemia, Monocytic, Acute / diagnosis*
  • Leukemia, Monocytic, Acute / genetics*
  • Myeloid-Lymphoid Leukemia Protein / genetics*
  • Skin Neoplasms / diagnosis
  • Translocation, Genetic*

Substances

  • KMT2A protein, human
  • Myeloid-Lymphoid Leukemia Protein
  • Histone-Lysine N-Methyltransferase