Genetic profiling of myeloproliferative disorders by single-nucleotide polymorphism oligonucleotide microarray Academic Article uri icon

Overview

MeSH Major

  • Gene Expression Profiling
  • Myeloproliferative Disorders
  • Oligonucleotide Array Sequence Analysis
  • Polymorphism, Single Nucleotide

abstract

  • Genomic abnormalities, including 9p uniparental disomy/JAK2 point mutations, 1p uniparental disomy/MPL point mutations, deletions of RB1 and NF1 are common alterations in MPD, especially in PMF.

publication date

  • November 2008

Research

keywords

  • Academic Article

Identity

Language

  • eng

PubMed Central ID

  • PMC5519083

Digital Object Identifier (DOI)

  • 10.1016/j.exphem.2008.06.006

PubMed ID

  • 18723266

Additional Document Info

start page

  • 1471

end page

  • 9

volume

  • 36

number

  • 11