Detection of amplified or deleted chromosomal regions
Abstract
The present invention relates to in situ hybridization methods for the identification of new chromosomal abnormalities associated with various diseases. In particular, it provides probes which are specific to a region of amplification in chromosome 20.
- Inventors:
-
- San Francisco, CA
- Walnut Creek, CA
- Issue Date:
- Research Org.:
- Lawrence Livermore National Laboratory (LLNL), Livermore, CA (United States)
- OSTI Identifier:
- 870192
- Patent Number(s):
- 5472842
- Assignee:
- Regents of University of California (Oakland, CA)
- Patent Classifications (CPCs):
-
C - CHEMISTRY C12 - BIOCHEMISTRY C12Q - MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS
Y - NEW / CROSS SECTIONAL TECHNOLOGIES Y10 - TECHNICAL SUBJECTS COVERED BY FORMER USPC Y10S - TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- DOE Contract Number:
- W-7405-ENG-48
- Resource Type:
- Patent
- Country of Publication:
- United States
- Language:
- English
- Subject:
- detection; amplified; deleted; chromosomal; regions; relates; situ; hybridization; methods; identification; abnormalities; associated; various; diseases; particular; provides; probes; specific; region; amplification; chromosome; 20; various diseases; chromosomal abnormalities; hybridization methods; situ hybridization; provides probes; abnormalities associated; chromosomal region; /435/999/
Citation Formats
Stokke, Trond, Pinkel, Daniel, and Gray, Joe W. Detection of amplified or deleted chromosomal regions. United States: N. p., 1995.
Web.
Stokke, Trond, Pinkel, Daniel, & Gray, Joe W. Detection of amplified or deleted chromosomal regions. United States.
Stokke, Trond, Pinkel, Daniel, and Gray, Joe W. Sun .
"Detection of amplified or deleted chromosomal regions". United States. https://www.osti.gov/servlets/purl/870192.
@article{osti_870192,
title = {Detection of amplified or deleted chromosomal regions},
author = {Stokke, Trond and Pinkel, Daniel and Gray, Joe W},
abstractNote = {The present invention relates to in situ hybridization methods for the identification of new chromosomal abnormalities associated with various diseases. In particular, it provides probes which are specific to a region of amplification in chromosome 20.},
doi = {},
journal = {},
number = ,
volume = ,
place = {United States},
year = {1995},
month = {1}
}
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