Patients' rights or family responsibilities? Two approaches to genetic testing

Med Law Rev. 1998 Spring;6(1):1-41. doi: 10.1093/medlaw/6.1.1.
No abstract available

Publication types

  • Comparative Study

MeSH terms

  • Australia
  • Canada
  • Contracts
  • Delivery of Health Care
  • Disclosure*
  • Duty to Warn
  • Family*
  • Freedom
  • Genetic Counseling
  • Genetic Diseases, Inborn
  • Genetic Predisposition to Disease
  • Genetic Privacy*
  • Genetic Research
  • Genetic Testing*
  • Genetics
  • Guidelines as Topic*
  • Human Rights*
  • Humans
  • Informed Consent
  • Insurance, Health
  • Insurance, Life
  • International Cooperation*
  • Internationality*
  • Legislation as Topic
  • Medical Records
  • Models, Theoretical
  • Moral Obligations*
  • Ownership
  • Patients
  • Pedigree*
  • Personal Autonomy
  • Physicians
  • Privacy*
  • Public Policy*
  • Social Control, Formal*
  • Social Responsibility*
  • State Government
  • Tissue Banks
  • Tissue Donors
  • Tissue and Organ Procurement
  • United Kingdom
  • United States