Article
Myeloid malignancies with acquired trisomy 21 as the sole cytogenetic change are clinically highly variable and display a heterogeneous pattern of copy number alterations and mutations.
European journal of haematology - 1 Feb 2012
Larsson Nina, Lilljebjörn Henrik, Lassen Carin, Johansson Bertil, Fioretos Thoas
Abstract excerpt
OBJECTIVES: Acquired trisomy 21 is one of the most common numerical abnormalities in acute myeloid leukemia (AML), myelodysplastic syndrome (MDS), myeloproliferative neoplasms (MPN), and MDS/MPN; however, little is known about its pathogenic impact, accompanying submicroscopic changes, and its relation to other clinical features. Furthermore, previous studies addressing this issue have mainly focused on cases in...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
