Crossref Citations
This article has been cited by the following publications. This list is generated based on data provided by
Crossref.
Murray, Thomas H.
and
Mendel, Norman T.
1995.
Introduction: The Genome Imperative.
Journal of Law, Medicine & Ethics,
Vol. 23,
Issue. 4,
p.
309.
YESLEY, MICHAEL S.
1997.
Genetic Privacy, Discrimination, and Social Policy: Challenges and Dilemmas.
Microbial & Comparative Genomics,
Vol. 2,
Issue. 1,
p.
19.
1997.
Reproductive Health LiteratureWatch.
Journal of Women's Health,
Vol. 6,
Issue. 3,
p.
349.
Lemmens, Trudo
1997.
“What About Your Genes?” Ethical, Legal, and Policy Dimensions of Genetics in the Workplace.
Politics and the Life Sciences,
Vol. 16,
Issue. 1,
p.
57.
Troy, Edwin S. Flores
1997.
The Genetic Privacy Act: An Analysis of Privacy and Research Concerns.
Journal of Law, Medicine & Ethics,
Vol. 25,
Issue. 4,
p.
256.
Bove, Catherine M.
Fry, Sara T.
and
MacDonald, Deborah J.
1997.
Presymptomatic and predisposition genetic testing: Ethical and social considerations.
Seminars in Oncology Nursing,
Vol. 13,
Issue. 2,
p.
135.
Driscoll, Kathleen M.
1998.
The Application of Genetic Knowledge: Ethical and Policy Implications.
AACN Clinical Issues: Advanced Practice in Acute and Critical Care,
Vol. 9,
Issue. 4,
p.
588.
Greely, Henry T.
1998.
LEGAL, ETHICAL, AND SOCIAL ISSUES IN HUMAN GENOME RESEARCH.
Annual Review of Anthropology,
Vol. 27,
Issue. 1,
p.
473.
McQueen, Matthew J.
1998.
Ethical and Legal Issues in the Procurement, Storage and Use of DNA.
cclm,
Vol. 36,
Issue. 8,
p.
545.
1998.
Professional Disclosure of Familial Genetic Information.
The American Journal of Human Genetics,
Vol. 62,
Issue. 2,
p.
474.
Padberg, Rose Mary
and
Flach, Jennifer
1999.
National efforts to improve the informed consent process.
Seminars in Oncology Nursing,
Vol. 15,
Issue. 2,
p.
138.
Grizzle, William
Grody, Wayne W.
Noll, Walter W.
Sobel, Mark E.
Stass, Sanford A.
Trainer, Thomas
Travers, Henry
and
Weedn, Victor
1999.
Recommended Policies for Uses of Human Tissue in Research, Education, and Quality Control.
Archives of Pathology & Laboratory Medicine,
Vol. 123,
Issue. 4,
p.
296.
Powers, Madison
2000.
Encyclopedia of Ethical, Legal and Policy Issues in Biotechnology.
Petrila, John
2001.
Genetic risk: the new frontier for the duty to warn*.
Behavioral Sciences & the Law,
Vol. 19,
Issue. 3,
p.
405.
Surbone, Antonella
2001.
Ethical implications of genetic testing for breast cancer susceptibility.
Critical Reviews in Oncology/Hematology,
Vol. 40,
Issue. 2,
p.
149.
Magnusson, Roger S
2002.
Regulating Genetic Privacy in the Online Health Information Era.
Health Information Management,
Vol. 30,
Issue. 4,
p.
13.
Leino‐Kilpi, Helena
Välimäki, Maritta
Dassen, Theo
Gasull, Maria
Lemonidou, Chryssoula
Scott, P. Anne
Arndt, Marianne
and
Kaljonen, Anne
2002.
Maintaining privacy on post‐natal wards: a study in five European countries.
Journal of Advanced Nursing,
Vol. 37,
Issue. 2,
p.
145.
Weisbrot, David
2003.
The Australian joint inquiry into the Protection of Human Genetic Information.
New Genetics and Society,
Vol. 22,
Issue. 1,
p.
89.
Sankar, Pamela
2003.
Genetic Privacy.
Annual Review of Medicine,
Vol. 54,
Issue. 1,
p.
393.
2004.
Ethics and Information Technology: A Case-Based Approach to a Health Care System in Transition.
p.
113.