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References
- 1.Bell J. The new genetics in clinical practice. BMJ. 1998;316:618–620. doi: 10.1136/bmj.316.7131.618. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.Masters CL, Beyreuther K. Science, medicine and the future: Alzheimer’s disease. BMJ. 1998;316:446–448. doi: 10.1136/bmj.316.7129.446. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.Hubbard R, Lewontin RC. Pitfalls of genetic testing. N Engl J Med. 1996;334:1192–1193. doi: 10.1056/NEJM199605023341812. [DOI] [PubMed] [Google Scholar]
- 4.Watson P, Marcus JN, Lynch HT. Prognosis of BRCA1 hereditary breast cancer. Lancet. 1998;351:304–305. doi: 10.1016/S0140-6736(98)22005-8. [DOI] [PubMed] [Google Scholar]
- 5.Healy B. BRCA genes: bookmaking, fortune telling and medical care. N Engl J Med. 1997. p. 336. :1448-9. [DOI] [PubMed] [Google Scholar]
- 6.Human Genetics Advisory Commission. The implications of genetic testing for insurance. London: Office of Science and Technology, 1997.
- 7.Harper PS, Clarke AJ. Genetics, society and clinical practice. Oxford: BIOS Scientific Publishers; 1997. pp. 15–29. [Google Scholar]
- 8.Brave new now [editorial]. Nature Genetics 1997;15:1-2. [DOI] [PubMed]
- 9.Morton NE. Hippocratic or hypocritic: birth pangs of an ethical code. Nature Genetics. 1998;18:18. doi: 10.1038/ng0198-18. [DOI] [PubMed] [Google Scholar]
- 10.Reilly PR, Boshar MF, Holtzman SH. Ethical issues in genetic research: disclosure and informed consent. Nature Genetics. 1997;15:16–20. doi: 10.1038/ng0197-16. [DOI] [PubMed] [Google Scholar]
- 11.Veatch RM. Consent, confidentiality, and research. New Engl J Med. 1997;336:869–870. doi: 10.1056/NEJM199703203361209. [DOI] [PubMed] [Google Scholar]
- 12.NHS Executive. Population screening for prostate cancer. Leeds: NHS Executive, 1997 (EL(97)12).