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

BACKGROUND: 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 geno...

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Autors principals: Gunnarsson, Rebeqa, Mansouri, Larry, Isaksson, Anders, Göransson, Hanna, Cahill, Nicola, Jansson, Mattias, Rasmussen, Markus, Lundin, Jeanette, Norin, Stefan, Buhl, Anne Mette, Smedby, Karin Ekström, Hjalgrim, Henrik, Karlsson, Karin, Jurlander, Jesper, Geisler, Christian, Juliusson, Gunnar, Rosenquist, Richard
Format: Artigo
Idioma:Inglês
Publicat: Ferrata Storti Foundation 2011
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Original Articles
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3148910/
https://ncbi.nlm.nih.gov/pubmed/21546498
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3324/haematol.2010.039768
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