| Literature DB >> 3234043 |
Abstract
Fluorescent in situ hybridization provides a fast method for detection of specific nucleic acid sequences. We have used high-resolution, single-color fluorescent in situ hybridization with a combination centromeric-telomeric DNA probe, specific for chromosome 1, to investigate the feasibility of simultaneous assessment of numerical and structural chromosome aberrations. The K562 leukemia cell line served as a model.Entities:
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Year: 1988 PMID: 3234043 DOI: 10.1159/000132622
Source DB: PubMed Journal: Cytogenet Cell Genet ISSN: 0301-0171