Method for the detection of chromosome structural abnormalities by in situ hybridization to fixed tissue
US5856089A · kind A · utility
59Cited by
3References
42Claims
0Family size
Assignee
Inventors
Key dates
| Filing date | Jul 22, 1994 |
| Grant date | Jan 5, 1999 |
| Priority date | — |
| Expiry date | Jul 22, 2014 |
Classification
- Technology area (CPC C)Chemistry; Metallurgy
- CPC primaryC12Q2600/156
- WIPO fieldBiotechnology
- WIPO sectorChemistry
Abstract
The present invention is directed to in situ hybridization methods using nucleic acid probes for single copy sequences for detecting chromosomal structural abnormalities in fixed tissue obtained from a patient suspected of having a chromosomal structural abnormality.
Source: USPTO / EPO open patent data. Objective bibliographic and citation counts.