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Original Article: Clinical

Lack of nucleophosmin mutation in patients with myelodysplastic syndrome and acute myeloid leukemia with chromosome 5 abnormalities

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Pages 2141-2144 | Received 04 May 2007, Accepted 04 Aug 2007, Published online: 01 Jul 2009

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Joyce J Ou & Adam Bagg. (2009) Diagnostic challenges in the myelodysplastic syndromes: the current and future role of genetic and immunophenotypic studies. Expert Opinion on Medical Diagnostics 3:3, pages 275-291.
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Florian NolteWolf-K Hofmann. (2010) Molecular mechanisms involved in the progression of myelodysplastic syndrome. Future Oncology 6:3, pages 445-455.
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Zhijian Qian, John M. Joslin, Thelma R. Tennant, Shalini C. Reshmi, David J. Young, Angela Stoddart, Richard A. Larson & Michelle M. Le Beau. (2010) Cytogenetic and genetic pathways in therapy-related acute myeloid leukemia. Chemico-Biological Interactions 184:1-2, pages 50-57.
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Rachel Rau & Patrick Brown. (2009) Nucleophosmin ( NPM1 ) mutations in adult and childhood acute myeloid leukaemia: towards definition of a new leukaemia entity . Hematological Oncology 27:4, pages 171-181.
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Brunangelo Falini, Paolo Sportoletti & Maria Paola Martelli. (2009) Acute myeloid leukemia with mutated NPM1: diagnosis, prognosis and therapeutic perspectives. Current Opinion in Oncology 21:6, pages 573-581.
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M. Jädersten & E. Hellström-Lindberg. (2009) Myelodysplastic syndromes: biology and treatment. Journal of Internal Medicine 265:3, pages 307-328.
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Brunangelo Falini. (2008) Acute Myeloid Leukemia with Mutated Nucleophosmin. Clinical Leukemia 2:3, pages 163-173.
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M T Andersen, M K Andersen, D H Christiansen & J Pedersen-Bjergaard. (2008) NPM1 mutations in therapy-related acute myeloid leukemia with uncharacteristic features. Leukemia 22:5, pages 951-955.
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