Our inheritance, our future: Their rights?

International Journal of Children's Rights

Volumn 13, Issue 1-2, 2005, Pages 255-272

  McLean, A M Sheila ^a   Mason, J Kenyon ^b  

^a UNIVERSITY OF GLASGOW   (United Kingdom)

^b UNIVERSITY OF EDINBURGH   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 84856905557     PISSN: 09275568     EISSN: 15718182     Source Type: Journal    
DOI: 10.1163/1571818054545312     Document Type: Article

References (22)

1. Anionwu, E.N. and Atkins, K. (2001) The Politics of Sickle Cell and Thalassaemia, Open University Press.
2. Barnicoat, A. (1997) ' Screening for fragile X syndrome: a model for genetic disorders?' 315 British Medical Journal 1174.
3. British Medical Association (1998) Human Genetics: Choice and Responsibility. Oxford University Press.
4. Danish Council (1993) Ethics and Mapping the Human Genome. Copehagen. Edwards, P.J. and Hall.
5. D.M.B. (1992), 'Screening, ethics and the law' 305 British Medical Journal 267.
6. Gostin, L.O. (1995) 'Genetic privacy' 23 Journal of Law, Medicine and Ethics 320.
7. Hellman, D. (2003) 'What Makes Genetic Discrimination Exceptional?' 29 American Journal of Law and Medicine 77.
8. Hoffmann, D.E. and Wulfsberg E.A. (1995) 'Testing children for genetic predispositions: Is it in their best interests?' 23 Journal of Law, Medicine & Ethics 331.
9. Hubbard, R. and Wald, E. (1993) Exploding the Gene Myth. Boston Beacon Press.
10. Laurie, G. (1999 (a)) 'Obligations arising from genetic information-negligence and the protection of family interests' (1999) 11 CFLQ 109.
11. -(1999 (b)) 'In defence of ignorance: Genetic information and the right not to know' 6 European Journal of Health Law 119.
12. -(2002) 'Better to hesitate at the threshold of compulsion: PKU testing and the concept of family autonomy in Eire' 28 Journal of Medical Ethics 136.
13. Maddox, J. (1991) 'The case for the human genome' 352 Nature 11.
14. Mueller, R.F. and Young, J.D. (1995) Emery's Elements of Medical Genetics (9th edition, 1995), Chapter 22.
15. Robertson, J. and Savulescu, J. (2001) 'Is there a case in favour of predictive genetic testing in young children?' 15 Bioethics 26.
16. Robinson, A. (1994) 'The Ethics of Gene Research' 150 Canadian Medical Association, J.721.
17. Ross, L.F. (2002) 'Predictive Genetic Testing for Conditions that present in Childhood' 12 Kennedy Institute of Ethics Journal 225.
18. Royal College of Physicians (1991) Ethical Issues in Clinical Genetics.
19. Streetley, A. (2000) 'A national policy for sickle cell disease and thalassaemia major for the United Kingdon' 320 British Medical Journal 1353.
20. White Paper (2003) Our Inheritance, Our Future Cm 5791 London, HMSO.
21. Whittaker, LA. (1992) 'The implications of the human genome project for family practice' 35 Journal of Family Practice 294.
22. Wolf, S. (1995) 'Beyond "genetic dicrimination": Toward the broader harm of geneticism' 23 Journal of Law, Medicine and Ethics 345.