Cooper, David Neil ORCID: https://orcid.org/0000-0002-8943-8484 and Clayton, John F.
1988.
DNA polymorphism and the study of disease associations.
Human Genetics
78
(4)
, pp. 299-312.
10.1007/BF00291724
|
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: | 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 |





Altmetric
Altmetric