NIH-DOE Working Group on Ethical, Legal, and Social Implications of Human Genome Research. (1993). Genetic information and health insurance: Report of the Task Force on Genetic Information and Insurance. National Institutes of Health, National Center for Human Genome Research.
File — Box: 74, Folder: 36
Scope and Contents
From the Series:
This series consists of grey literature collected by Capron. It contains material produced by governmental agencies and non-governmental organizations and includes technical reports, working papers, policy briefs, white papers, and newsletters, as well as conference proceedings and abstracts. Topics covered include death and dying, aging, human cloning, research ethics, the human genome, stem cells, HIV/AIDS, and reproduction.
Dates
- From the Series: Creation: 1967 - 2018
Conditions Governing Access
The collection is open for research use.
Manuscript reviews are restricted for 75 years from date of creation.
Language of Materials
From the Collection: English
Repository Details
Part of the Bioethics Research Library Archives Repository