Array CGH identifies copy number changes in 11% of 520 MDS patients with normal karyotype and uncovers prognostically relevant deletions

Leukemia. 2016 Jan;30(1):257-60. doi: 10.1038/leu.2015.257. Epub 2015 Sep 22.

Authors

S Volkert¹, T Haferlach¹, J Holzwarth¹, M Zenger¹, W Kern¹, M Staller¹, Y Nagata², K Yoshida², S Ogawa², S Schnittger¹, C Haferlach¹

Affiliations

¹ MLL Munich Leukemia Laboratory, Munich, Germany.
² Department of Pathology and Tumor Biology, Kyoto University, Kyoto, Japan.

PMID: 26392226
DOI: 10.1038/leu.2015.257

No abstract available

Publication types

Letter

MeSH terms

Adolescent
Adult
Aged
Aged, 80 and over
Child
Comparative Genomic Hybridization / methods*
Female
Gene Dosage*
Humans
Karyotype
Male
Middle Aged
Myelodysplastic Syndromes / genetics*
Prognosis
Sequence Deletion*