- (1 other version)The jurisprudence of genetic privacy.Tony McGleenan - 1998 - Medicine, Health Care and Philosophy 1 (3):225-233.details
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Eugenics and Mandatory Informed Prenatal Genetic Testing: A Unique Perspective from China.Zhang Di, Vincent H. Ng, Zhaochen Wang, Xiaomei Zhai & Reidar K. Lie - 2015 - Developing World Bioethics 16 (2):107-115.details
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Personal utility in genomic testing: is there such a thing?Eline M. Bunnik, A. Cecile J. W. Janssens & Maartje H. N. Schermer - 2015 - Journal of Medical Ethics 41 (4):322-326.details
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(1 other version)Genetisches Screening und Ethik: Europäische Perspektiven : Ein Bericht über das EUROSCREEN I Projekt. [REVIEW]Ruth Chadwick, Henk ten Have, Jorgen Husted, Mairi Levit, Tony McGleenan, Darren Shickle & Urban Wiesing - 1998 - Ethik in der Medizin 10 (3):195-202.details
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Preimplantation genetic diagnosis and the 'new' eugenics.D. S. King - 1999 - Journal of Medical Ethics 25 (2):176-182.details
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Palliative care ethics: non-provision of artificial nutrition and hydration to terminally ill sedated patients.R. Gillon - 1994 - Journal of Medical Ethics 20 (3):131-187.details
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(1 other version)The jurisprudence of genetic privacy.Tony McGleenan - 1998 - Medicine, Health Care and Philosophy 1 (3):225-233.details
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A Capabilities Approach to Prenatal Screening for Fetal Abnormalities.Guido Wert, Peter Schröder-Bäck, Wybo Dondorp & Greg Stapleton - 2019 - Health Care Analysis 27 (4):309-321.details
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Ethics of genetic screening: the first report of the Nuffield Council on Bioethics.R. Gillon - 1994 - Journal of Medical Ethics 20 (2):67-92.details
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Would you rather be a 'birth' or a 'genetic' mother? If so, how much?J. G. Thornton, H. M. McNamara & I. A. Montague - 1994 - Journal of Medical Ethics 20 (2):87-92.details
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Commercialisation of genetic diagnostic services.Rogeer Hoedemaekers & Henk ten Have - 1998 - Medicine, Health Care and Philosophy 1 (3):217-224.details
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(1 other version)Informed consent and genetic information.O. O'Neill - 2001 - Studies in History and Philosophy of Science Part C: Studies in History and Philosophy of Biological and Biomedical Sciences 32 (4):689-704.details
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The Right to Know and the Right Not to Know Revisited: Part One.Roger Brownsword & Jeff Wale - 2017 - Asian Bioethics Review 9 (1-2):3-18.details
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Legal Conceptions: Regulating Gametes and Gamete Donation.Kath O'Donnell - 2000 - Health Care Analysis 8 (2):137-154.details
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Regulating Risk: Defining Genetic Privacy in the United States and Britain.Shobita Parthasarathy - 2004 - Science, Technology, and Human Values 29 (3):332-352.details
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Prospects for limiting access to prenatal genetic information about Down syndrome in light of the expansion of prenatal genomics.Chris Kaposy - 2022 - The New Bioethics 29 (3):226-246.details
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Eugenics and the New Genetics in Britain: Examining Contemporary Professionals' Accounts.Amanda Amos, Sarah Cunningham-Burley & Anne Kerr - 1998 - Science, Technology and Human Values 23 (2):175-198.details
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Ethics, Genetic Technologies and Equine Sports: The Prospect of Regulation of a Modified Therapeutic Use Exemption Policy.M. L. H. Campbell & M. J. McNamee - 2021 - Sport, Ethics and Philosophy 15 (2):227-250.details
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Genetic Testing and Private Insurance – A Case of “Selling One’s Body”?D. Hübner - 2005 - Medicine, Health Care and Philosophy 9 (1):43-55.details
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A Capabilities Approach to Prenatal Screening for Fetal Abnormalities.Greg Stapleton, Wybo Dondorp, Peter Schröder-Bäck & Guido de Wert - 2019 - Health Care Analysis 27 (4):309-321.details
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Philosophy, freedom and the public good: a review and analysis of 'Public Health Ethics' Holland, S. (2007).Andrew Miles & Michael Loughlin - 2009 - Journal of Evaluation in Clinical Practice 15 (5):838-858.details
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The ethics of genetic screening: the first report of the Nuffield Council on Bioethics: another personal view.D. Shapiro - 1994 - Journal of Medical Ethics 20 (3):185-187.details
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