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Use of fluorescent in situ hybridization to confirm trisomy of chromosome region 1q32-qter as the sole karyotypic defect in a colon cancer cell line

✍ Scribed by Darren K. Griffin; Sarah E. A. Leigh; Dr. Joy D. A. Delhanty


Publisher
John Wiley and Sons
Year
1990
Tongue
English
Weight
278 KB
Volume
1
Category
Article
ISSN
1045-2257

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✦ Synopsis


The sole chromosome defect in a colon cancer cell line derived from a patient with inherited nonpolyposis colorectal cancer was karyotypically designated as 46,XY,-I3,+der( I3)t( I; I3)(q32. I ;p I I) on the basis of banding homology. We have obtained molecular confirmation that the additional chromosome material is derived from chromosome region I q32-qter by the use of a highly specific fluorescent in situ hybridisation technique on G-banded chromosomes and also by Southern hybridisation.