Skip to main content
Article thumbnail
Location of Repository

Molecular allelokaryotyping of T-cell prolymphocytic leukemia cells with high density single nucleotide polymorphism arrays identifies novel common genomic lesions and acquired uniparental disomy

By Daniel Nowak, Emilie Le Toriellec, Marc-Henri Stern, Norihiko Kawamata, Tadayuki Akagi, Martin J. Dyer, Wolf-Karsten Hofmann, Seishi Ogawa and H. Phillip Koeffler


T-cell prolymphocytic leukemia is a rare aggressive lymphoproliferative disease with a mature T-cell phenotype and characteristic genomic rearrangements of 14q11. This study identifies numerous new potential target genes in common breakpoints, deletions and regions of acquired uniparental disomy

Topics: Original Article
Publisher: Ferrata Storti Foundation
OAI identifier:
Provided by: PubMed Central
Download PDF:
Sorry, we are unable to provide the full text but you may find it at the following location(s):
  • http://www.pubmedcentral.nih.g... (external link)
  • Suggested articles

    To submit an update or takedown request for this paper, please submit an Update/Correction/Removal Request.