Array-based genomic screening at diagnosis and during follow-up in chronic lymphocytic leukemia

Rebeqa Gunnarsson, Larry Mansouri, Anders Isaksson, Hanna Göransson, Nicola Cahill, Mattias Jansson, Markus Rasmussen, Jeanette De Sparra Lundin, Stefan Norin, Anne Mette Buhl, Karin Ekström Smedby, Henrik Hjalgrim, Karin Karlsson, Jesper Jurlander, Christian Geisler, Gunnar Juliusson, Richard Rosenquist

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87 Citationer (Scopus)

Abstract

High-resolution genomic microarrays enable simultaneous detection of copy-number aberrations such as the known recurrent aberrations in chronic lymphocytic leukemia [del(11q), del(13q), del(17p) and trisomy 12], and copy-number neutral loss of heterozygosity. Moreover, comparison of genomic profiles from sequential patients' samples allows detection of clonal evolution.
OriginalsprogEngelsk
TidsskriftHaematologica
Vol/bind96
Udgave nummer8
Sider (fra-til)1161-9
Antal sider9
ISSN0390-6078
DOI
StatusUdgivet - 2011

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