Genome-wide genotyping of acute myeloid leukemia with translocation t(9;11)(p22;q23) reveals novel recurrent genomic alterations

Haematologica. 2014 Aug;99(8):e133-5. doi: 10.3324/haematol.2014.105544. Epub 2014 May 23.

Affiliations

¹ Department of Internal Medicine III, University of Ulm, Germany.
² Microarray Core Facility, University of Ulm, Germany.
³ Department of Internal Medicine III, University of Ulm, Germany [email protected].

No abstract available

Keywords: acute myeloid leukemia; copy number alterations; genotyping; novel recurrent genomic alterations; t(9;11)(p22;q23).

Publication types

Letter

MeSH terms

Adult
Chromosomes, Human, Pair 11 / genetics*
Chromosomes, Human, Pair 9 / genetics*
Cohort Studies
Female
Genome-Wide Association Study / methods*
Genomics / methods*
Humans
Leukemia, Myeloid, Acute / diagnosis
Leukemia, Myeloid, Acute / genetics*
Male
Polymorphism, Single Nucleotide / genetics
Translocation, Genetic / genetics*