Genomics
Author:
Publisher
Springer International Publishing
Link
https://link.springer.com/content/pdf/10.1007/978-3-319-09483-0_214
Reference9 articles.
1. Boddington, P. (2012). Ethical challenges in genomics research. Heidelberg: Springer.
2. Bovenberg, J. (2005). Whose tissue is it anyway? Nature Biotechnology, 23, 229–233. doi:10.1038/nbt0805-929.
3. Dondorp, W., Sikkema-Raddatz, B., Die-Smulders, C., & de Wert, G. (2012). Arrays in postnatal and prenatal diagnosis: An exploration of the ethics of consent. Human Mutation, 33(6), 916–922. doi:10.1002/humu.22068.
4. Geller, G., Dvoskin, R., Thio, C. L., Duggal, P., Lewis, M. H., Bailey, T. C., Sutherland, A., Salmon, D. A., & Kahn, J. P. (2014). Genomics and infectious disease: A call to identify the ethical, legal and social implications for public health and clinical practice. Genome Medicine, 6, 106. doi:10.1186/s13073-014-0106-2.
5. Howard, H., Knoppers, B. M., & Borry, P. (2010). Blurring lines. The research activities of direct-to-consumer genetic testing companies raise questions about consumers as research subjects. EMBO Reports, 11(8), 579–582. doi:10.1038/embor.2010.105.
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