Whole-exome sequencing in del(5q) myelodysplastic syndromes in transformation to acute myeloid leukemia

Leukemia. 2014 May;28(5):1148-51. doi: 10.1038/leu.2013.381. Epub 2013 Dec 24.

Authors

A Pellagatti¹, M Fernandez-Mercado¹, C Di Genua¹, M J Larrayoz², S Killick³, H Dolatshad¹, A Burns⁴, M J Calasanz², A Schuh⁴, J Boultwood¹

Affiliations

¹ LLR Molecular Haematology Unit, Nuffield Division of Clinical Laboratory Sciences, Radcliffe Department of Medicine, University of Oxford, Oxford, UK.
² Department of Genetics, University of Navarra, Pamplona, Spain.
³ Department of Haematology, Royal Bournemouth Hospital, Bournemouth, UK.
⁴ NIHR Biomedical Research Centre, University of Oxford, Oxford, UK.

PMID: 24365791
DOI: 10.1038/leu.2013.381

No abstract available

Publication types

Letter
Research Support, Non-U.S. Gov't

MeSH terms

Chromosome Deletion*
Chromosomes, Human, Pair 5*
Exome*
Humans
Leukemia, Myeloid, Acute / genetics*
Myelodysplastic Syndromes / genetics*

Grants and funding

Wellcome Trust/United Kingdom