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International Journal of Laboratory Hematology, ISSN 1751-5521, 02/2020, Volume 42, Issue 1, pp. 37 - 45
Introduction A prototype of good prognosis, t(8;21)‐positive AML, has diverse clinical and genetic features which affect its outcome. This study aimed at... 
morphology | cytogenetics | RUNX1‐RUNX1T1 AML | prognosis
Journal Article
Journal of Cancer Research and Clinical Oncology, ISSN 0171-5216, 11/2019, Volume 145, Issue 11, pp. 2871 - 2874
Journal Article
International Journal of Cancer, ISSN 0020-7136, 02/2017, Volume 140, Issue 3, pp. 653 - 661
Journal Article
Journal of Clinical and Experimental Hematopathology, ISSN 1346-4280, 2014, Volume 54, Issue 2, pp. 167 - 170
Journal Article
Cancer, ISSN 0008-543X, 08/2018, Volume 124, Issue 16, pp. 3329 - 3338
Background Mutations in the colony‐stimulating factor 3 receptor (CSF3R) gene occur frequently in chronic neutrophilic leukemia and are rare in de novo acute... 
runt‐related transcription factor 1 (RUNX1)‐RUNX1 translocation partner 1 (RUNX1‐RUNX1T1) | core‐binding factor β subunit‐myosin heavy‐chain 11 (CBFB‐MYH11) | colony‐stimulating factor 3 receptor (CSF3R) | acute myeloid leukemia | CCAAT/enhancer binding protein α (CEBPA) | core-binding factor β subunit-myosin heavy-chain 11 (CBFB-MYH11) | colony-stimulating factor 3 receptor (CSF3R) | runt-related transcription factor 1 (RUNX1)-RUNX1 translocation partner 1 (RUNX1-RUNX1T1) | CHRONIC NEUTROPHILIC LEUKEMIA | SEVERE CONGENITAL NEUTROPENIA | SECONDARY | CLASSIFICATION | CCAAT/enhancer binding protein alpha (CEBPA) | WORLD-HEALTH-ORGANIZATION | core-binding factor beta subunit-myosin heavy-chain 11 (CBFB-MYH11) | RECEPTOR MUTATIONS | C/EBP-ALPHA | ONCOLOGY | ACUTE LYMPHOBLASTIC-LEUKEMIA | PATIENT | MICE | Leukemia, Myeloid, Acute - pathology | Humans | Middle Aged | Child, Preschool | Infant | Male | Core Binding Factor beta Subunit - genetics | Young Adult | Receptors, Colony-Stimulating Factor - genetics | Adolescent | Aged, 80 and over | Adult | Female | Aged | CCAAT-Enhancer-Binding Proteins - genetics | Mutation | Nuclear Proteins - genetics | Child | Core Binding Factor Alpha 2 Subunit - genetics | Leukemia, Myeloid, Acute - therapy | Leukemia, Myeloid, Acute - genetics | Transcription factors | Acute lymphatic leukemia | RNA-directed DNA polymerase | Myeloid leukemia | Leukemia | Abnormalities | Genes | Runx1 protein | Leukocytes (neutrophilic) | CCAAT/enhancer-binding protein | Lymphatic leukemia | Patients | Gene sequencing | Proteins | Polymerase chain reaction | Genetic abnormalities | Alterations | Missense mutation | Acute myeloid leukemia
Journal Article
Journal of Clinical and Experimental Hematopathology, ISSN 1346-4280, 2015, Volume 55, Issue 3, pp. 181 - 185
The t(8;21)(q22;q22) translocation is specifically observed in acute myeloid leukemia (AML) M2 subtype, whereas del(5q) is one of the most common cytogenetic... 
chromosome aberrations | acute myeloid leukemia | coexistence | RUNX1/RUNX1T1 | 5q deletion
Journal Article
International Journal of Hematology, ISSN 0925-5710, 8/2018, Volume 108, Issue 2, pp. 208 - 212
Journal Article