Bioethics in the United Kingdom: Genetic Screening, Disability Rights, and the Erosion of Trust
Cambridge Quarterly of Healthcare Ethics 12 (03) (2003)
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Ron Amundson & Shari Tresky (2007). On a Bioethical Challenge to Disability Rights. Journal of Medicine and Philosophy 32 (6):541 – 561.
Marcia Riordan (2012). Maternal Serum Testing: Is Invasive Testing a Passing Era. Bioethics Research Notes 24 (1):7.
Susan Lindee & Rebecca Mueller (2011). Is Cystic Fibrosis Genetic Medicine's Canary? Perspectives in Biology and Medicine 54 (3):316-331.
Bruce Guthrie (2008). Trust and Asymmetry in General Practitioner-Patient Relationships in the United Kingdom. In Julie Brownlie, Alexandra Greene & Alexandra Howson (eds.), Researching Trust and Health. Routledge.
S. Camporesi (2010). Choosing Deafness with PHD: An Ethical Way to Carry on a Cultural Bloodline? Cambridge Quarterly Healthcare Ethics 19 (1):86-96.
Anita Ho (2007). Disability in the Bioethics Curriculum. Teaching Philosophy 30 (4):403-420.
Anita Ho (2007). Disability in the Bioethics Curriculum. Teaching Philosophy 30 (4):403-420.
Ron Amundson & Shari Tresky (2008). Bioethics and Disability Rights: Conflicting Values and Perspectives. Journal of Bioethical Inquiry 5 (2/3):111-123.
J. Stuart Horner (2000). Autonomy in the Medical Profession in the United Kingdom – an Historical Perspective. Theoretical Medicine and Bioethics 21 (5).
Ruth Chadwick, Henk ten Have, Jfrgen Husted, Mairi Levitt, Tony McGleenan, Darren Shickle & Urban Wiesing (1998). Genetic Screening and Ethics: European Perspectives. Journal of Medicine and Philosophy 23 (3):255 – 273.
Burke K. Zimmerman (1991). Human Germ-Line Therapy: The Case for its Development and Use. Journal of Medicine and Philosophy 16 (6):593-612.
Sahin Aksoy (2001). Antenatal Screening and its Possible Meaning From Unborn Baby's Perspective. BMC Medical Ethics 2 (1):1-11.
Robert H. Blank (1982). Public Policy Implications of Human Genetic Technology: Genetic Screening. Journal of Medicine and Philosophy 7 (4):355-374.
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