Ethical Dilemmas in Testing for Late Onset Conditions: Reactions to Testing and Perceived Impact on Other Family Members

Author:

Chapman Elizabeth1

Affiliation:

1. ; Centre for Family Research; University of Cambridge; Cambridge United Kingdom

Publisher

Wiley

Subject

Genetics(clinical)

Reference32 articles.

1. A world-wide assessment of the frequency of suicide, suicide attempts, or psychiatric hospitalisation after predictive testing for Huntington disease;Almquuist;Am J Hum Genet,1999

2. Genetic information and “Genetic Identity.”;Ashcroft,1999

3. Psychological impact of population-based carrier testing for cystic fibrosis: 3 year follow-up;Axworthy;Lancet,1996

4. United Kingdom experience with presymptomatic testing of individuals at 25% risk for Huntington's disease;Benjamin;Clin Genet,2000

5. Future directions in genetic counseling: Practical and ethical considerations;Biesecker-Bowles;Kennedy Inst Ethics J,1998

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