| Literature DB >> 9739022 |
M L Larramendy1, M Virolainen, E Tukiainen, I Elomaa, S Knuutila.
Abstract
DNA sequence copy number changes were studied by comparative genomic hybridization (CGH) in 28 desmoid tumors. Changes were detected in 12 tumors (43%) with a mean of 1.4 changes per sample (range: 1 to 7). Out of 12 tumors associated with pregnancy or Gardner's syndrome, only two displayed changes. The minimal common regions of the most frequent gains were 1q21 (39%), chromosome 20 (32%), and 9p12 (21%). No high-level amplifications were detected. Losses of DNA sequences were two times less frequent than gains and the minimal common regions of the most frequent losses were 6q16-q21 (14%), 5q14 (11%), and 13q21-q31 (11%).Entities:
Mesh:
Year: 1998 PMID: 9739022 DOI: 10.1002/(sici)1098-2264(199810)23:2<183::aid-gcc12>3.0.co;2-p
Source DB: PubMed Journal: Genes Chromosomes Cancer ISSN: 1045-2257 Impact factor: 5.006