Ethical issues and policy analysis for genetic testing: Huntington's disease as a paradigm for diseases with a late onset

Human Reproduction and Genetic Ethics 11 (2):28 (2005)
  Copy   BIBTEX

Abstract

This article has no associated abstract. (fix it)

Links

PhilArchive



    Upload a copy of this work     Papers currently archived: 92,283

External links

  • This entry has no external links. Add one.
Setup an account with your affiliations in order to access resources via your University's proxy server

Through your library

Similar books and articles

The Ethics of Krabbe Newborn Screening.R. H. Dees & J. M. Kwon - 2013 - Public Health Ethics 6 (1):114-128.
Huntington disease: prenatal screening for late onset disease.J. Greenberg - 1993 - Journal of Medical Ethics 19 (2):121-121.
Genetic testing of children for late onset disease.Mary Ann Sevick, Donna G. Nativio & Terrance Mcconnell - 2005 - Cambridge Quarterly of Healthcare Ethics 14 (1):47-56.
Predictive genetic testing for conditions that present in childhood.Lainie Friedman Ross - 2002 - Kennedy Institute of Ethics Journal 12 (3):225-244.
How distinctive is genetic information?M. Richards - 2001 - Studies in History and Philosophy of Science Part C: Studies in History and Philosophy of Biological and Biomedical Sciences 32 (4):663-687.
Genetic disease, genetic testing and the clinician.Kelly C. Smith - 2001 - Journal of the American Medical Association 285 (1):91.

Analytics

Added to PP
2013-10-30

Downloads
3 (#1,715,951)

6 months
1 (#1,478,781)

Historical graph of downloads
How can I increase my downloads?

References found in this work

No references found.

Add more references