Trisomy 13 correlates with RUNX1 mutation and increased FLT3 expression in AML-M0 patients-Reference-Cited by-同舟云学术

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Trisomy 13 correlates with RUNX1 mutation and increased FLT3 expression in AML-M0 patients

Published:2007-08-01 Issue:8 Volume:92 Page:1123-1126
ISSN:0390-6078
Container-title:Haematologica
language:en
Short-container-title:Haematologica

Author:

Silva F. P.G.,Lind A.,Brouwer-Mandema G.,Valk P. J.M.,Giphart-Gassler M.

Publisher

Ferrata Storti Foundation (Haematologica)

Subject

Hematology

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3. Clinico-pathologic characteristics and outcomes of the World Health Organization (WHO) provisional entity de novo acute myeloid leukemia with mutated RUNX1;Modern Pathology;2020-04-01

4. Comparison of mutational profiles and clinical outcomes in patients with acute myeloid leukemia with mutated RUNX1 versus acute myeloid leukemia with myelodysplasia-related changes with mutated RUNX1;Leukemia & Lymphoma;2020-02-24

5. Clinical and molecular characterization of patients with acute myeloid leukemia and sole trisomies of chromosomes 4, 8, 11, 13 or 21;Leukemia;2019-08-28

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