Choosing Deafness with Preimplantation Genetic Diagnosis: An Ethical Way to Carry on a Cultural Bloodline?
Cambridge Quarterly of Healthcare Ethics 19 (01):86- (2009)
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S. Camporesi (2010). Choosing Deafness with PHD: An Ethical Way to Carry on a Cultural Bloodline? Cambridge Quarterly Healthcare Ethics 19 (1):86-96.
John Mcmillan (2008). Choosing Between Possible Lives: Law and Ethics of Prenatal and Preimplantation Genetic Diagnosis - by R. Scott. Journal of Applied Philosophy 25 (4):355-357.
Mary B. Mahowald (2000). Christian Munthe, Pure Selection: The Ethics of Preimplantation Genetic Diagnosis and Choosing Children Without Abortion. Theoretical Medicine and Bioethics 21 (4).
Janet Malek & Judith Daar (2012). The Case for a Parental Duty to Use Preimplantation Genetic Diagnosis for Medical Benefit. American Journal of Bioethics 12 (4):3-11.
C. Cameron (2003). Is There an Ethical Difference Between Preimplantation Genetic Diagnosis and Abortion? Journal of Medical Ethics 29 (2):90-92.
Tanja Krones & Gerd Richter (2004). Preimplantation Genetic Diagnosis (PGD): European Perspectives and the German Situation. Journal of Medicine and Philosophy 29 (5):623 – 640.
Thomas S. Petersen (2005). Just Diagnosis? Preimplantation Genetic Diagnosis and Injustices to Disabled People. Journal of Medical Ethics 31 (4):231-234.
Jeffrey R. Botkin (1998). Ethical Issues and Practical Problems in Preimplantation Genetic Diagnosis. Journal of Law, Medicine and Ethics 26 (1):17-28.
Patrick Giam (2012). Preimplantation Genetic Diagnosis: A Perspective From Human Dignity`. Bioethics Research Notes 24 (3):40.
Helen Watt (2004). Preimplantation Genetic Diagnosis: Choosing the “Good Enough” Child. Health Care Analysis 12 (1):51-60.
E. Turillazzi & V. Fineschi (2008). Preimplantation Genetic Diagnosis: A Step by Step Guide to Recent Italian Ethical and Legislative Troubles. Journal of Medical Ethics 34 (10):e21-e21.
D. S. King (1999). Preimplantation Genetic Diagnosis and the 'New' Eugenics. Journal of Medical Ethics 25 (2):176-182.
E. Asscher & B.-J. Koops (2009). The Right Not to Know and Preimplantation Genetic Diagnosis for Huntington's Disease. Journal of Medical Ethics 36 (1):30-33.
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