Ethical implications of genetic information

Online Journal of Issues in Nursing

Volumn 6, Issue 2 SPEC. ISS., 2001, Pages 72-77

  Jenkins, Jean ^a  

^a NONE

Author keywords

Ethics; Genetic services

Indexed keywords

BEHAVIOR; CONFIDENTIALITY; FAMILY; GENETIC ANALYSIS; GENETIC SCREENING; GENETICS; GENOTYPE; HEALTH CARE; HEALTH CARE FINANCING; HEALTH CARE POLICY; HEALTH CARE QUALITY; HEALTH PRACTITIONER; HEALTH SERVICE; HEREDITY; HUMAN; INFORMED CONSENT; MEDICAL DECISION MAKING; MEDICAL ETHICS; MEDICAL INFORMATION; MEDICAL PRACTICE; MEDICAL RECORD; MEDICAL TECHNOLOGY; NURSING EDUCATION; OUTCOMES RESEARCH; PATIENT CARE; PATIENT REFERRAL; PHILOSOPHY; QUALITY CONTROL; RESOURCE MANAGEMENT; REVIEW; SOCIAL ASPECT; WELLBEING;

EID: 3242670644     PISSN: 10913734     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review

References (11)

1. Alliance of Genetic Support Groups. (1997). Informed consent: Participation in genetic research studies. Chevy Chase, MD: Alliance of Genetic Support Groups. Available [online] http://www.geneticalliance.org/Resources/ Publications/infoconsent.html
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8. Hudson, K. L., Rothenberg, K. H., Andrews, L. B., Kahn, M. J. E., Collins, F. S. (1995). Genetic discrimination and health insurance: An urgent need for reform. Science, 270, 391-393.
9. Lapham, E., Kozma, C., & Weiss, J. (1996). Genetic discrimination: Perspectives of consumers. Science, 274, 621-624.
10. Rieger, P., & Pentz, R. (1999). Genetic testing and informed consent. Seminars in Oncology Nursing, 15(2), 104-115.
11. st century: Incorporating genetics into primary health care. New York: Cold Spring Harbor Laboratory Press.