Quantification of rareNPM1mutation subtypes by digital PCR
Author:
Affiliation:
1. MLL Munich Leukaemia Laboratory; Munich Germany
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/bjh.13038/fullpdf
Reference10 articles.
1. Evaluation of different NPM1 mutations in AML patients according to clinical, cytogenetic and molecular features and impact on outcome;Alpermann;Blood,2013
2. Cytoplasmic nucleophosmin in acute myelogenous leukemia with a normal karyotype;Falini;New England Journal of Medicine,2005
3. Quantitative assessment of minimal residual disease in acute myeloid leukemia carrying nucleophosmin (NPM1) gene mutations;Gorello;Leukemia,2006
4. Monitoring of minimal residual disease in NPM1-mutated acute myeloid leukemia: a study from the German-Austrian acute myeloid leukemia study group;Krönke;Journal of Clinical Oncology,2011
5. Absolute quantitative detection of ABL tyrosine kinase domain point mutations in chronic myeloid leukemia using a novel nanofluidic platform and mutation-specific PCR;Oehler;Leukemia,2009
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