Disclosure of Huntington's Disease to Family Members: The Dilemma of Known but Unknowing Parties
Author:
Affiliation:
1. Unit for Health Rights and Ethics, Gertner Institute for Epidemiology and Health Policy Research, Sheba Medical Center, Tel Hashomer 52621, Israel.
Publisher
Mary Ann Liebert Inc
Subject
Genetics (clinical)
Link
http://www.liebertpub.com/doi/pdf/10.1089/109065700750065090
Reference6 articles.
1. Prediction of psychological functioning one year after the predictive test for Huntington's disease and impact of the test result on reproductive decision making.
2. The evolving duty to disclose the presence of genetic disease to relatives
3. The new genetics: Genetic testing and public policy
4. Attitudes of persons at risk for Huntington disease toward predictive testing
5. In Defence of Ignorance: Genetic Information and the Right not to Know
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4. Genetic counseling and testing for Huntington's disease: A historical review;American Journal of Medical Genetics Part B: Neuropsychiatric Genetics;2016-05-13
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