The 8p11 myeloproliferative syndrome owing to rare FGFR1OP2-FGFR1 fusion

Eur J Haematol. 2011 Apr;86(4):347-9. doi: 10.1111/j.1600-0609.2010.01568.x. Epub 2011 Feb 18.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Adult
  • Chromosome Painting
  • Chromosomes, Human, Pair 12 / genetics
  • Chromosomes, Human, Pair 8 / genetics*
  • Humans
  • Male
  • Myeloproliferative Disorders / genetics*
  • Oncogene Proteins, Fusion / genetics*
  • Proto-Oncogene Proteins / genetics*
  • Receptor, Fibroblast Growth Factor, Type 1 / genetics*
  • Syndrome
  • Translocation, Genetic

Substances

  • CEP43 protein, human
  • Oncogene Proteins, Fusion
  • Proto-Oncogene Proteins
  • FGFR1 protein, human
  • Receptor, Fibroblast Growth Factor, Type 1