[HTML][HTML] A case of acute myeloid leukemia (AML) with an unreported combination of chromosomal abnormalities: gain of isochromosome 5p, tetrasomy 8 and …

C Paar, G Herber, D Voskova, M Fridrik, H Stekel… - Molecular …, 2013 - Springer
Background Acute myeloid leukemia (AML) comprises a spectrum of myeloid malignancies
which are often associated with distinct chromosomal abnormalities, and the analysis of …

[HTML][HTML] A de novo acute myeloid leukemia (AML-M4) case with a complex karyotype and yet unreported breakpoints

W Al-Achkar, A Aljapawe, MAK Othman, A Wafa - Molecular Cytogenetics, 2013 - Springer
Background Acute myelogeneous leukemia (AML) is a malignancy of the hematopoietic
stem cells, for which cytogenetic analysis is still one of the most important diagnostic and …

[引用][C] A novel translocation, t (3; 20)(q13; p13), in acute monocytic leukemia

B Qian, Z Sun, Z Wu, H Liu… - Cancer genetics and …, 2009 - cancergeneticsjournal.org
Because an increasing number of chromosomal aberrations have been detected in the
patients with acute leukemia, cytogenetic findings have become more valuable in …

[HTML][HTML] A rare case of acute myeloid leukemia with t (12; 19)(q13; q13)

A Chebly, FG Haddad, J Bassil, T Yammine… - Leukemia Research …, 2020 - Elsevier
Acute myeloid leukemia (AML) is characterized by chromosomal abnormalities affecting
both prognosis and course of treatment. While most AML patients have well described …

[HTML][HTML] Two rare cases of acute myeloid leukemia with t (8; 16)(p11. 2; p13. 3) and 1q duplication: case presentation and literature review

M Liu, Y Ren, X Wang, X Lu, M Li, YM Kim, S Li… - Molecular …, 2020 - Springer
Background Acute myeloid leukemia (AML) is a complex hematological disease
characterized by genetic and clinical heterogeneity. The identification and understanding of …

[HTML][HTML] Acute myeloid leukemia, M1 with trisomy 1, 8, and 21: a case report of a rare complex karyotype

AH Abdelrahman, EA Hasan… - The Egyptian Journal …, 2016 - journals.lww.com
Conclusion Reports of trisomy 1 in AML are rare, and, to the best of our knowledge, the
present case is the only one reported with the occurrence of trisomy 1 in addition to trisomy 8 …

Novel chromosome 16 abnormality—der (16) del (16)(q13) t (16; 21)(p11. 2; q22)—Associated with acute myeloid leukemia

P Sharma, N Watson, L Robson, J Gallo… - Cancer genetics and …, 1999 - Elsevier
Inversion of chromosome 16 is a common feature of acute myeloid leukemia (AML) M4,
while t (16; 21), although also associated with AML, appears to be a separate entity. We …

Translocation t (5; 18)(q35; q21) as a rare nonrandom abnormality in acute myeloid leukemia

A Daraki, LK Bourantas, KN Manola - Cytogenetic and Genome …, 2013 - karger.com
Cytogenetic abnormalities play an important role in diagnosis, classification and prognosis
in acute myeloid leukemia (AML). Nevertheless, several chromosome abnormalities have …

Duplication 15q in a patient with t (8; 21) acute myeloblastic leukemia (M2)

L Zhang, JJ Mulvihill, GT Kinasewitz, KV Scott… - Cancer genetics and …, 2002 - Elsevier
We present unique chromosomal abnormalities found in a patient with acute myeloblastic
leukemia (AML) of French–American–British subtype M2. The patient was referred for an …

[HTML][HTML] Atypical chromosome abnormalities in acute myeloid leukemia type M4

AC Fett-Conte, RV Estrela… - … and molecular biology, 2007 - SciELO Brasil
This study reports an adult AML-M4 patient with atypical chromosomal aberrations present
in all dividing bone marrow cell at diagnosis: t (1; 8)(p32. 1; q24. 2), der (9) t (9; 10)(q22;?) …