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Investigation of 305 patients with myelodysplastic syndromes and 20q deletion for associated cytogenetic and molecular genetic lesions and their prognostic impact.
Bacher U, Haferlach T, Schnittger S, Zenger M, Meggendorfer M, Jeromin S, Roller A, Grossmann V, Krauth MT, Alpermann T, Kern W, Haferlach C. Bacher U, et al. Among authors: alpermann t. Br J Haematol. 2014 Mar;164(6):822-33. doi: 10.1111/bjh.12710. Epub 2013 Dec 26. Br J Haematol. 2014. PMID: 24372512 Free article.
Quantification of rare NPM1 mutation subtypes by digital PCR.
Bacher U, Dicker F, Haferlach C, Alpermann T, Rose D, Kern W, Haferlach T, Schnittger S. Bacher U, et al. Among authors: alpermann t. Br J Haematol. 2014 Dec;167(5):710-4. doi: 10.1111/bjh.13038. Epub 2014 Jul 18. Br J Haematol. 2014. PMID: 25039748 Free article. No abstract available.
106 results