The medium and the message : tissue samples, genetic information and data protection
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Søren Holm (2001). The Privacy of Tutankhamen – Utilising the Genetic Information in Stored Tissue Samples. Theoretical Medicine and Bioethics 22 (5).
Margaret Otlowski (2007). Donor Perspectives on Issues Associated with Donation of Genetic Samples and Information: An Australian Viewpoint. Journal of Bioethical Inquiry 4 (2).
Richard A. Spinello (2004). Property Rights in Genetic Information. Ethics and Information Technology 6 (1):29-42.
Xinqing Zhang, Kenji Matsui, Benjamin Krohmal, Alaa Zeid, Vasantha Muthuswamy, Young Koo, Yoshikuni Kita & Reidar K. Lie (2010). Attitudes Towards Transfers of Human Tissue Samples Across Borders: An International Survey of Researchers and Policy Makers in Five Countries. BMC Medical Ethics 11 (1):16-.
Karen J. Maschke (2010). Wanted: Human Biospecimens. Hastings Center Report 40 (5):21-23.
Asya Al-Riyami, Deepali Jaju, Sanjay Jaju & Henry J. Silverman (2011). The Adequacy of Informed Consent Forms in Genetic Research in Oman: A Pilot Study. Developing World Bioethics 11 (2):57-62.
Peter Hustinx (2010). Privacy by Design: Delivering the Promises. Identity in the Information Society 3 (2):253-255.
Christiane Auray-Blais & Johane Patenaude (2006). A Biobank Management Model Applicable to Biomedical Research. BMC Medical Ethics 7 (1):1-9.
Neil C. Manson (2006). What is Genetic Information, and Why is It Significant? A Contextual, Contrastive, Approach. Journal of Applied Philosophy 23 (1):1–16.
Soraj Hongladarom (2009). Privacy, the Individual and Genetic Information: A Buddhist Perspective. Bioethics 23 (7):403-412.
Loretta M. Kopelman (1994). Informed Consent and Anonymous Tissue Samples: The Case of Hiv Seroprevalence Studies. Journal of Medicine and Philosophy 19 (6):525-552.
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