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Constitutional C-band polymorphism in lymphocytes from patients with chronic myeloid leukemia.

Abstract
The C-band heterochromatin polymorphism of chromosomes 1, 9, and 16 was studied in lymphocytes from 53 patients with Ph1-positive chronic myeloid leukemia (CML) and 183 control persons. The patients had significantly larger heterochromatic blocks on chromosome 16 (p less than 0.01) and fewer partial inversions of chromosome 9 (p less than 0.05) than the control persons, whereas no differences were found for the symmetry/asymmetry pattern. We suggest that the increased constitutive heterochromatin regions may, via sister chromosome exchange, facilitate homo- or hemizygotization of genes which favor neoplasia development and/or progression.
AuthorsU Kristoffersson, A Bernheim, R Berger, B Nilsson, S Heim, N Mandahl, F Mitelman
JournalHereditas (Hereditas) Vol. 110 Issue 2 Pg. 145-8 ( 1989) ISSN: 0018-0661 [Print] England
PMID2745151 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Heterochromatin
Topics
  • Chromosome Aberrations
  • Chromosome Banding
  • Chromosome Inversion
  • Chromosomes, Human, Pair 1 (ultrastructure)
  • Chromosomes, Human, Pair 16 (ultrastructure)
  • Chromosomes, Human, Pair 9 (ultrastructure)
  • Heterochromatin (ultrastructure)
  • Humans
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive (genetics)
  • Polymorphism, Genetic
  • Sister Chromatid Exchange

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