Acute myeloid leukemia patients with variant or unusual translocations involving chromosomes 8 and 21–A comprehensive cytogenetic profiling of three cases with …
TVA Raj, P Gopinath, JAG Raj… - Journal of Cancer …, 2022 - journals.lww.com
Background: t (8; 21)(q22; q22) is the most frequent recurrent translocation in acute myeloid
leukemia (AML) resulting in an in-frame fusion of RUNX1/RUNX1T1 that regulates various …
leukemia (AML) resulting in an in-frame fusion of RUNX1/RUNX1T1 that regulates various …
Identification of chromosomal abnormalities and genomic features in near-triploidy/tetraploidy-acute leukemia by fluorescence in situ hybridization
R Yang, M Jiang, J Zhao, H Chen, J Gong… - Cancer Management …, 2019 - Taylor & Francis
Background Near-triploidy/tetraploidy is rarely found in acute leukemia. Only limited data are
available to characterize this condition, and it remains largely unknown. Patients and …
available to characterize this condition, and it remains largely unknown. Patients and …
Down Syndrome Resulting from a Rare non-Robertsonian Translocation t (11; 21)(p13; q22)
DBA Rosan, PL Dourado, AE Ruiz… - Archives Health …, 2021 - ahs.famerp.br
Introduction: Down syndrome (DS) is a common genetic disorder, occurring in approximately
1 in 700 births. It results from an extra copy (triplication) of the whole or part of the long arm …
1 in 700 births. It results from an extra copy (triplication) of the whole or part of the long arm …
[HTML][HTML] A Novel Cytogenetic Variant Translocation in Acute Myeloid Leukemia
MV Patel, SN Vaniawala, PK Gadhia - Journal of Case Reports, 2017 - casereports.in
Background: Acute myeloid leukemia (AML) is a heterogeneous group of malignant
neoplasm of hematopoietic disorders characterized by an abnormal proliferation of myeloid …
neoplasm of hematopoietic disorders characterized by an abnormal proliferation of myeloid …
[PDF][PDF] Sindrome de Down resultante de uma translocação não Robertsoniana rara t (11; 21)(p13; q22)
DBA Rosan, PL Dourado, AE Ruiz, V CC, F da Silva… - ahs.famerp.br
Introdução: A síndrome de Down (SD) é um distúrbio genético comum, ocorrendo em
aproximadamente 1 em 700 nascimentos. Resulta de uma cópia extra de todo ou de parte …
aproximadamente 1 em 700 nascimentos. Resulta de uma cópia extra de todo ou de parte …