Genetic alterations in patients with chronic leucocytosis and persistent thrombocytosis
Author:
Funder
Japan Society for the Promotion of Science
Publisher
Springer Science and Business Media LLC
Subject
Genetics
Link
https://link.springer.com/content/pdf/10.1007/s12041-021-01354-7.pdf
Reference19 articles.
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2. Gambacorti-Passerini C. B., Donadoni C., Parmiani A., Pirola A., Redaelli S., Signore G. et al. 2015 Recurrent ETNK1 mutations in atypical chronic myeloid leukemia. Blood 125, 499–503.
3. Genovese G., Kähler A. K., Handsaker R. E., Lindberg J., Rose S. A., Bakhoum S. F. et al. 2014 Clonal hematopoiesis and blood-cancer risk inferred from blood DNA sequence. N. Engl. J. Med. 371, 2477–2487.
4. Herishanu Y., Rogowski O., Polliack A. and Marilus R. 2006 Leukocytosis in obese individuals: possible link in patients with unexplained persistent neutrophilia. Eur. J. Haematol. 76, 516–520.
5. Hoischen A., van Bon B. W., Gilissen C., Arts P., van Lier B., Steehouwer M. et al. 2010 De novo mutations of SETBP cause Schinzel-Giedion syndrome. Nat. Genet. 42, 483–485.
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