Submicroscopic deletion of FGFR1 gene is recurrently detected in myeloid and lymphoid neoplasms associated with ZMYM2-FGFR1 rearrangements: a case study

Acta Haematol. 2012;127(2):119-23. doi: 10.1159/000334707. Epub 2012 Jan 11.
No abstract available

Publication types

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

MeSH terms

  • Base Sequence
  • Chromosome Deletion
  • Chromosomes, Human, Pair 8 / genetics
  • DNA-Binding Proteins / genetics*
  • Fatal Outcome
  • Gene Deletion*
  • Gene Rearrangement*
  • Humans
  • Male
  • Middle Aged
  • Molecular Sequence Data
  • Myeloproliferative Disorders / genetics*
  • Receptor, Fibroblast Growth Factor, Type 1 / genetics*
  • Transcription Factors / genetics*

Substances

  • DNA-Binding Proteins
  • Transcription Factors
  • ZMYM2 protein, human
  • FGFR1 protein, human
  • Receptor, Fibroblast Growth Factor, Type 1

Supplementary concepts

  • Chromosome 8p deletion syndrome (partial)