Detection of male cells in mixtures containing varying proportions of male and female cells by fluorescence in situ hybridization and G-banding
β Scribed by A. Denise White; Marion C. Sweeney
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- English
- Weight
- 520 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0196-4763
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
## Abstract The i(12p) marker chromosome has been found to be a highly nonrandom chromosome abnormality associated with germ cell tumors (GCTs). We have previously shown that a chromosome 12 centromere specific Ξ±βsatellite DNA probe detects the i(12p) by virtue of differences in the size of the sig
## BACKGROUND. Benign body cavity effusions sometimes cannot be distinguished from malignant ones by conventional cytology. The authors performed fluores-Barry Sanchez, B
Triple fluorescence in situ hybridization with a plasmid DNA library from sorted human chromosomes 8 in combination with bacteriophage clones flanking the breakpoint in 8q24 of the Burkitt lymphoma cell line )I was used for the specific delineation of this breakpoint in individual tumor cells. With
## BACKGROUND. Chromosomal abnormalities in some lymphomas are associated with a poor prognosis. Trisomy 12 and deletions of chromosome 13 have been described in small lymphocytic lymphoma (SLL). To determine whether chromosomal aberrations could be detected by fluorescence in situ hybridization (F