Informed Consent and Genetic Research
Clayton, Ellen Wright
Anonymous Testing; Confidentiality; Consent; Disclosure; DNA; DNA Data Banks; Data Banks; Discrimination; Family Members; Genetic Information; Genetic Research; Genetic Screening; Human Experimentation; Informed Consent; Insurance; Mass Screening; Newborns; Parental Consent; Pedigree; Records; Research; Research Subjects; Risks and Benefits; Social Discrimination; Stigmatization; Tissue Banks;
Showing items related by title, author, creator and subject.
Kelsey, Karl T.; Li, Frederick P.; Polli, Anita M.; Clayton, Ellen Wright (1996-04-10)
Clayton, Ellen Wright; Steinberg, Karen K.; Khoury, Muin J.; Thomson, Elizabeth; Andrews, Lori; Kahn, Mary Jo Ellis; Kopelman, Loretta M.; Weiss, Joan O. (1995-12-13)
Genetic Testing is Different [reviews of GENETIC TESTING FOR ALZHEIMER DISEASE: ETHICAL AND CLINICAL ISSUES, by Stephen G. Post and Peter J. Whitehouse and PROMOTING SAFE AND EFFECTIVE GENETIC TESTING IN THE UNITED STATES: PRINCIPLES AND RECOMMENDATIONS, by Task Force on Genetic Testing, NIH-DOE Working Group on Ethical, Legal, and Social Implications of Human Genome Research] Clayton, Ellen Wright (2001-04)