The 8p11 anomaly in “monoblastic” leukaemia
Author:
Publisher
Elsevier BV
Subject
Cancer Research,Oncology,Hematology
Reference14 articles.
1. Chromosome pattern, occupation, and clinical features in patients with acute nonlymphocytic leukemia;Mitelman;Cancer Genet. Cytogenet.,1981
2. Malignant histiocytosis. Clinical and cytogenetic studies in a newborn and a child;Shouten;Cancer,1983
3. Chromosomes patterns in 26 South African children with acute nonlymphocytic leukemia;Bernstein;Cancer Genet. Cytogenet.,1984
4. A unique 8;16 translocation in two infants with poorly differentiated monoblastic leukemia;Bernstein;Cancer Genet. Cytogenet.,1987
5. A new specific chromosomal rearrangement, t(8;16) (pll;pl3), in acute monocytic leukaemia;Heim;Br. J. Haemat.,1987
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1. De novo monocytic-M5b AML with t(8;16) (p11.2; p13.3) KAT6A/CREBBP fusion and FLT3-TKD mutation complicated by chemotherapy-induced Takotsubo cardiomyopathy;BMJ Case Reports;2023-03
2. Therapy-related Myeloid Leukemia With the Translocation t(8;19)(p11;q13) Leading to a KAT6A-LEUTX Fusion Gene;Anticancer Research;2021-04
3. Acute Myeloid Leukemia in an Infant with t(8;19)(p11.2;q13) Translocation: Case Report and a Review of the Literature;Case Reports in Hematology;2019-09-08
4. Leukemia Cells Directly Phagocytose Blood Cells in AML-Associated Hemophagocytic Lymphohistiocytosis: A Case Report and Review of the Literature;Acta Haematologica;2014-09-16
5. The leucine twenty homeobox (LEUTX) gene, which lacks a histone acetyltransferase domain, is fused toKAT6Ain therapy-related acute myeloid leukemia with t(8;19)(p11;q13);Genes, Chromosomes and Cancer;2014-01-21
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