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Mutations in SETBP1 are recurrent in myelodysplastic syndromes and often coexist with cytogenetic markers associated with disease progression

✍ Scribed by Fernandez-Mercado, Marta; Pellagatti, Andrea; Di Genua, Cristina; Larrayoz, Maria Jose; Winkelmann, Nils; Aranaz, Paula; Burns, Adam; Schuh, Anna; Calasanz, Maria Jose; Cross, Nicholas C. P.; Boultwood, Jacqueline

Book ID: 120654104
Publisher: John Wiley and Sons
Year: 2013
Tongue: English
Weight: 72 KB
Category: Article
ISSN: 0007-1048
DOI: 10.1111/bjh.12491

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