De novo acute myeloid leukemia with t(8;21)(q22;q22) and monosomy 7

The t(8: 21)(q22;q22) is the most common cytogenetic abnormality, usually with a favorable risk, in acute myeloid leukemia (AML). This translocation is not only of diagnostic significance but also has impact on survival outcomes and therapeutic implications. However, patients with adverse outcome in...

Full description

Saved in:
Bibliographic Details
Main Authors: Harish Kumar, Paresh Singhal, Ajay Malik, Sanjeevan Sharma
Format: Artigo
Language:Inglês
Published: Wolters Kluwer Medknow Publications 2019-01-01
Series:Journal of Applied Hematology
Subjects:
acute myeloid leukemia
monosomy 7
t(8;21)
Online Access:http://www.jahjournal.org/article.asp?issn=1658-5127;year=2019;volume=10;issue=3;spage=99;epage=102;aulast=Kumar
Tags: Add Tag
No Tags, Be the first to tag this record!

Similar Items