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Chromosome abnormalities involving heterochromatic regions in monocytic leukemia.

作者信息

Rege-Cambrin G, Kerim S, Scaravaglio P, Michaux J L, Van den Berghe H, Saglio G

机构信息

Dipartimento di Scienze Biomediche e Oncologia Umana, Università di Torino, Italy.

出版信息

Cancer Genet Cytogenet. 1990 May;46(1):99-106. doi: 10.1016/0165-4608(90)90015-3.

Abstract

We report two cases of monocytic leukemia associated with cytogenetic changes involving the juxtacentromeric heterochromatin of different chromosomes. In a patient with chronic myelomonocytic leukemia (CMMoL) we describe a translocation t(1;9)(q12;q13) in which the duplicated derivative chromosome 9q + showed a huge centromeric C-band, derived by fusion of the heterochromatic regions of chromosomes 1 and 9. The constitutional karyotype showed two heterochromatin polymorphisms, 1qh + and inv(9qh). In the second case, an acute monoblastic leukemia was associated with an abnormally elongated juxtacentromeric heterochromatic region of chromosome 4 that was not constitutionally present.

摘要

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