National symposium on problems of presymptomatic testing for Huntington's disease, Cardiff
Journal of Medical Ethics 16 (1):41-42 (1990)
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Mariam Ghosn (2007). Predictive Testing for Huntington's Disease in Adolescents: Part 2. Chisholm Health Ethics Bulletin 12 (3):3.
Mariam Ghosn (2007). Predictive Testing for Huntington's Disease in Young Children: Part I. Chisholm Health Ethics Bulletin 12 (3):1.
Lainie Friedman Ross (2002). Predictive Genetic Testing for Conditions That Present in Childhood. Kennedy Institute of Ethics Journal 12 (3):225-244.
M. Huggins & M. R. Hayden (1992). Predictive Testing for Huntington Disease. Journal of Medical Ethics 18 (1):47-48.
Kathryn Edge (2013). The Benefits and Potential Harms of Genetic Testing for Huntington's Disease: A Case Study. Human Reproduction and Genetic Ethics 14 (2):14 - 19.
Lisa Bortolotti & Heather Widdows (2011). The Right Not to Know: The Case of Psychiatric Disorders. Journal of Medical Ethics 37 (11):673-676.
J. Greenberg (1993). Huntington Disease: Prenatal Screening for Late Onset Disease. Journal of Medical Ethics 19 (2):121-121.
S. G. Post (1992). Huntington's Disease: Prenatal Screening for Late Onset Disease. Journal of Medical Ethics 18 (2):75-78.
R. E. Duncan (2005). Ethical Considerations in Presymptomatic Testing for Variant CJD. Journal of Medical Ethics 31 (11):625-630.
R. H. Dees & J. M. Kwon (2013). The Ethics of Krabbe Newborn Screening. Public Health Ethics 6 (1):114-128.
N. Nijsingh (2013). Krabbe Newborn Screening: The Issue of Informed Consent. Public Health Ethics 6 (1):126-128.
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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