Cooper, David Neil ![]() |
Official URL: http://dx.doi.org/10.1007/BF00291724
Abstract
Recombinant DNA approaches to disease analysis may be as applicable to studies of disease association as they are to the analysis and diagnosis of single-gene defects. Population and/or family association analyses, using restriction fragment length polymorphisms around candidate genes as markers, have been employed to study conditions such as atherosclerosis and disease with an HLA-association. Progress made to date in disease-association studies using recombinant DNA methodology is reviewed, the rationale behind such studies is examined and associated problems and pitfalls discussed.
Item Type: | Article |
---|---|
Date Type: | Publication |
Status: | Published |
Schools: | Medicine |
Subjects: | R Medicine > R Medicine (General) |
Publisher: | Springer |
ISSN: | 0340-6717 |
Last Modified: | 27 Oct 2022 08:21 |
URI: | https://orca.cardiff.ac.uk/id/eprint/62065 |
Citation Data
Cited 81 times in Scopus. View in Scopus. Powered By Scopus® Data
Actions (repository staff only)
![]() |
Edit Item |