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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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| Autori principali: | , , , , , , , , , , , , , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Ferrata Storti Foundation
2011
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| Soggetti: | |
| Accesso online: | 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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