2000
DOI: 10.1590/s1415-47572000000400060
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Centromeric, pericentromeric and heterochromatin abnormalities in chromosomal rearrangements of human leukemia

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“…Besides these common cytogenetic abnormalities, there are some rare variants of translocations such as dicentric chromosomes [2]. In human leukemia, recurrent and clonal dicentric chromosomes have been found to be associated with some subtypes of leukemia, such as dic(5;17) and dic(17;18) in myeloid cell proliferations, and dic(7;9), dic(9;12) and dic(9;20) in acute lymphoblastic leukemias [6]. We report a case of acute myeloblastic leukemia with a dic(1;15)(p11;p11), resulting in trisomy of the long arm of chromosome 1.…”
Section: Discussionmentioning
confidence: 99%
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“…Besides these common cytogenetic abnormalities, there are some rare variants of translocations such as dicentric chromosomes [2]. In human leukemia, recurrent and clonal dicentric chromosomes have been found to be associated with some subtypes of leukemia, such as dic(5;17) and dic(17;18) in myeloid cell proliferations, and dic(7;9), dic(9;12) and dic(9;20) in acute lymphoblastic leukemias [6]. We report a case of acute myeloblastic leukemia with a dic(1;15)(p11;p11), resulting in trisomy of the long arm of chromosome 1.…”
Section: Discussionmentioning
confidence: 99%
“…However, the translocation breakpoints are likely to be in heterochromatic regions. Heterochromatin could have roles in centromere architecture and the prevention of merotely, but the possible consequences of heterochromatin rearrangements are still a question mark [6]. Heterochromatin rearrangements (partial trisomies and monosomies) cause imbalance by silencing genes placed in the region of chromosomal breakpoints due to the translocation of heterochromatin to ectopic location [14].…”
Section: Discussionmentioning
confidence: 99%