Ethical concerns in the research and treatment of complex disease

This publication has 19 references indexed in Scilit:

• Genetic information and life insurance: A proposal for an ethical European policy
  Social Science & Medicine, 1995
• Genetic testing for children and adolescents. Who decides?
  JAMA, 1994
• Familial Coercion to Participate in Genetic Family Studies: Is There Cause for IRB Intervention?
  IRB: Ethics & Human Research, 1994
• Ethical Issues in Genetic Testing for Alzheimerʼs Disease
  Alzheimer Disease & Associated Disorders, 1994
• Genetic Information and Health Insurance: Report of the Task Force on Genetic Information and Insurance. NIH/DOE Working Group on Ethical, Legal, and Social Implications of Human Genome Research
  Human Gene Therapy, 1993
• Consensus Guidelines for the Management of Insulin‐dependent (Type 1) Diabetes
  Diabetic Medicine, 1993
• Research samples from families with genetic diseases: a proposed code of conduct.
  BMJ, 1993
• Opioids and behavior: genetic aspects
  Cellular and Molecular Life Sciences, 1988
• A burning issue. Health and wealth up in smoke
  Archives of internal medicine (1960), 1986
• HIGH‐RISK WORKERS OR HIGH‐RISK WORK? GENETIC SUSCEPTIBILITY POLICIES IN THE HAZARDOUS WORKPLACE
  International Journal of Sociology and Social Policy, 1986