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The clinical path to integrated genomics in ALL

In this issue of Blood, Moorman et al show that most good-risk patients can now be classified robustly by integrating the information from prevalent copy-number alterations (CNAs) in relevant combinations and classical cytogenetic risk factors in acute lymphoblastic leukemia (ALL).(1)

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awdur: Bourquin, Jean-Pierre
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: American Society of Hematology 2014
Pynciau:
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC4148753/
https://ncbi.nlm.nih.gov/pubmed/25170109
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2014-07-585927
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