Quantification of subclonal distributions of recurrent genomic aberrations in paired pre-treatment and relapse samples from patients with B-cell chronic lymphocytic leukemia

Genome-wide array approaches and sequencing analyses are powerful tools for identifying genetic aberrations in cancers, including leukemias and lymphomas. However, the clinical and biological significance of such aberrations and their subclonal distribution are poorly understood. Here, we present th...

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Detalles Bibliográficos
Autores principales: Knight, S J L, Yau, C, Clifford, R, Timbs, A T, Sadighi Akha, E, Dréau, H M, Burns, A, Ciria, C, Oscier, D G, Pettitt, A R, Dutton, S, Holmes, C C, Taylor, J, Cazier, J-B, Schuh, A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2012
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3505832/
https://www.ncbi.nlm.nih.gov/pubmed/22258401
http://dx.doi.org/10.1038/leu.2012.13

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3505832/
https://www.ncbi.nlm.nih.gov/pubmed/22258401
http://dx.doi.org/10.1038/leu.2012.13

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