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Characterization of 35 new cases with four different MPLW515 mutations and essential thrombocytosis or primary myelofibrosis.
Schnittger S, Bacher U, Haferlach C, Beelen D, Bojko P, Bürkle D, Dengler R, Distelrath A, Eckart M, Eckert R, Fries S, Knoblich J, Köchling G, Laubenstein HP, Petrides P, Planker M, Pihusch R, Weide R, Kern W, Haferlach T. Schnittger S, et al. Among authors: kern w. Haematologica. 2009 Jan;94(1):141-4. doi: 10.3324/haematol.13224. Epub 2008 Nov 23. Haematologica. 2009. PMID: 19029146 Free PMC article. No abstract available.
[Diagnosis of leukemia using microarray technology].
Kohlmann A, Schoch C, Schnittger S, Kern W, Haferlach T. Kohlmann A, et al. Among authors: kern w. Dtsch Med Wochenschr. 2002 Oct 18;127(42):2216-22. doi: 10.1055/s-2002-34945. Dtsch Med Wochenschr. 2002. PMID: 12397553 German. No abstract available.
Acute myeloid leukemia with recurring chromosome abnormalities as defined by the WHO-classification: incidence of subgroups, additional genetic abnormalities, FAB subtypes and age distribution in an unselected series of 1,897 patients with acute myeloid leukemia.
Schoch C, Schnittger S, Kern W, Dugas M, Hiddemann W, Haferlach T. Schoch C, et al. Among authors: kern w. Haematologica. 2003 Mar;88(3):351-2. Haematologica. 2003. PMID: 12651278 No abstract available.
AML with 11q23/MLL abnormalities as defined by the WHO classification: incidence, partner chromosomes, FAB subtype, age distribution, and prognostic impact in an unselected series of 1897 cytogenetically analyzed AML cases.
Schoch C, Schnittger S, Klaus M, Kern W, Hiddemann W, Haferlach T. Schoch C, et al. Among authors: kern w. Blood. 2003 Oct 1;102(7):2395-402. doi: 10.1182/blood-2003-02-0434. Epub 2003 Jun 12. Blood. 2003. PMID: 12805060 Free article.
1,197 results