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  1. Antenatal Genetic Testing and the Right to Remain in Ignorance.Bennett Rebecca - 2001 - Theoretical Medicine and Bioethics 22 (5):461-471.
    As knowledge increases about the human genome,prenatal genetic testing will become cheaper,safer and more comprehensive. It is likelythat there will be a great deal of support formaking prenatal testing for a wide range ofgenetic disorders a routine part of antenatalcare. Such routine testing is necessarilycoercive in nature and does not involve thesame standard of consent as is required inother health care settings. This paper askswhether this level of coercion is ethicallyjustifiable in this case, or whether pregnantwomen have a right to (...)
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  • The Need to Know—Therapeutic Privilege: A Way Forward. [REVIEW]Kate Hodkinson - 2013 - Health Care Analysis 21 (2):105-129.
    Providing patients with information is fundamental to respecting autonomy. However, there may be circumstances when information may be withheld to prevent serious harm to the patient, a concept referred to as therapeutic privilege. This paper provides an analysis of the ethical, legal and professional considerations which impact on a decision to withhold information that, in normal circumstances, would be given to the patient. It considers the status of the therapeutic privilege in English case law and concludes that, while reference is (...)
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