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Published online before print April 10, 2008
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Commentary |
From the Department of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, Pennsylvania
Abstract
This Commentary highlights two articles that focus on molecular techniques to identify mutations in nucleophosmin (NPM1), which is the most frequently mutated gene in cytogenetically normal acute myeloid leukemia (CN-AML)
This article has been cited by other articles:
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M. L. Gulley, T. C. Shea, and Y. Fedoriw Genetic Tests To Evaluate Prognosis and Predict Therapeutic Response in Acute Myeloid Leukemia J. Mol. Diagn., January 1, 2010; 12(1): 3 - 16. [Abstract] [Full Text] [PDF] |
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