Journal article

Genetic testing without consent: the implications of the new Human Tissue Act 2004.

Publication status:: Published

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APA Style

Lucassen, A., & Kaye, J. (2006). Genetic testing without consent: the implications of the new Human Tissue Act 2004. Journal of Medical Ethics, 32(12), 690–692.

MLA Style

Lucassen, A., and J. Kaye. “Genetic Testing without Consent: the Implications of the New Human Tissue Act 2004.” Journal of Medical Ethics, vol. 32, no. 12, 2006, pp. 690–92.

Chicago Style

Lucassen, A, and J Kaye. 2006. “Genetic Testing without Consent: the Implications of the New Human Tissue Act 2004.” Journal of Medical Ethics 32 (12): 690–92.
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Publisher copy:: 10.1136/jme.2005.013631

Authors

+ Lucassen, A More by this author

Role:: Author

+ Kaye, J More by this author

Role:: Author

Journal:: Journal of medical ethics More from this journal
Volume:: 32
Issue:: 12
Pages:: 690-692
Publication date:: 2006-12-01
DOI:: 10.1136/jme.2005.013631
EISSN:: 1473-4257
ISSN:: 0306-6800

Language:: English
Keywords:: Access to Information

Genetic Predisposition to Disease

Humans

Great Britain

Genetic Privacy

Disclosure

Legislation, Medical

Ethics, Medical

Genetic Testing
Pubs id:: pubs:163614
UUID:: uuid:4d31f769-7a7e-45bc-b93b-ff475b6f4cd5
Local pid:: pubs:163614
Source identifiers:: 163614
Deposit date:: 2012-12-19

Terms of use

Copyright date:: 2006

Licence:: Terms and Conditions of Use for Oxford University Research Archive

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