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Title: Detection of amplified or deleted chromosomal regions

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. 3 figs.
Inventors:
; ;
Issue Date:
OSTI Identifier:
170470
Assignee:
Univ. of California, Oakland, CA (United States) PTO; SCA: 550900; PA: EDB-96:030779; SN: 96001517634
Patent Number(s):
US 5,472,842/A/
Application Number:
PAN: 8-132,808
Contract Number:
W-7405-ENG-48
Resource Relation:
Other Information: PBD: 5 Dec 1995
Research Org:
University of California
Country of Publication:
United States
Language:
English
Subject:
55 BIOLOGY AND MEDICINE, BASIC STUDIES; CHROMOSOMAL ABERRATIONS; DNA HYBRIDIZATION; HEREDITARY DISEASES; GENE AMPLIFICATION; CHROMOSOMES; CONGENITAL DISEASES