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Genetic defects in PRC2 components other than EZH2 are not common in myeloid malignancies

  • Leonie I Kroeze
  • , Gorica Nikoloski
  • , Pedro da Silva-Coelho
  • , Patricia van Hoogen
  • , Ellen Stevens-Linders
  • , Roland P Kuiper
  • , Susanne Schnittger
  • , Torsten Haferlach
  • , Heike L Pahl
  • , Bert A van der Reijden
  • , Joop H Jansen

Research output: Contribution to journalArticlepeer-review

15 Citations (Scopus)
Original languageEnglish
Pages (from-to)1318-9
Number of pages2
JournalBlood
Volume119
Issue number5
DOIs
Publication statusPublished - 2 Feb 2012
Externally publishedYes

Keywords

  • Carrier Proteins/genetics
  • Cohort Studies
  • DNA-Binding Proteins/genetics
  • Enhancer of Zeste Homolog 2 Protein
  • Gene Frequency
  • Genetic Predisposition to Disease
  • Genetic Variation/physiology
  • Hematologic Neoplasms/genetics
  • Humans
  • Myelodysplastic Syndromes/genetics
  • Myeloproliferative Disorders/genetics
  • Neoplasm Proteins
  • Nuclear Proteins/genetics
  • Polycomb Repressive Complex 2
  • Polycomb-Group Proteins
  • Polymorphism, Single Nucleotide
  • Repressor Proteins/genetics
  • Transcription Factors/genetics

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