Public Education Critical to Population-Wide Genomics Research

Friedrich discusses the development of a number of large-scale genetic databanks for the molecular study of disease. For these programs to succeed, the public must be included because human subjects are necessary to provide biological specimens.

Saved in:
Bibliographic Details
Published inJNCI : Journal of the National Cancer Institute Vol. 96; no. 16; pp. 1196 - 1197
Main Author Friedrich, M. J.
Format Journal Article
LanguageEnglish
Published United States Oxford University Press 18.08.2004
Oxford Publishing Limited (England)
Subjects
Bioethical Issues
Bioethics - education
Cancer
Community Participation
Databases, Genetic - ethics
Databases, Genetic - legislation & jurisprudence
Genetic Research - ethics
Genetic Research - legislation & jurisprudence
Genomics
Guidelines as Topic
Human Genome Project
Human subjects
Humans
National Institutes of Health (U.S.)
Research centers
United States
Wisconsin
Online AccessGet full text
ISSN0027-8874
1460-2105
1460-2105
DOI10.1093/jnci/96.16.1196

Cover

More Information
Summary:Friedrich discusses the development of a number of large-scale genetic databanks for the molecular study of disease. For these programs to succeed, the public must be included because human subjects are necessary to provide biological specimens.
Bibliography:istex:F922D474F15A85294E82E9611E1B99E10AEE4565
ark:/67375/HXZ-T8ZJ2R3Q-1
local:0961196
SourceType-Scholarly Journals-1
ObjectType-News-1
content type line 14
content type line 23
ISSN:0027-8874
1460-2105
1460-2105
DOI:10.1093/jnci/96.16.1196