Publisher
Springer Science and Business Media LLC
Subject
Health Policy,Education,Health(social science)
Reference53 articles.
1. Boenink, Marianne. 2008. Genetic diagnostics for hereditary breast cancer—displacement of uncertainty and responsibility. In Genetics from laboratory to society, ed. Gerard de Vries and Klasien Horstman, 37–63. Houndmills Basingstoke: Palgrave/Macmillan.
2. Bowker, Geoffrey C., and Susan Leigh Star. 2000. Sorting things out classification and its consequences. Cambridge: The MIT Press.
3. Chadwick, Ruth. 1997. The philosophy of the right to know and the right not to know. In The right to know and the right not to know, ed. R. Chadwick, M. Levitt, and D. Shickle, 13–22. Averbury: Aldershot.
4. Chadwick, Ruth, and Sarah Wilson. 2004. Genomic databases as public goods? Res Publica 10 (2): 123–134.
5. Chanock, Stephen, and Sholom Wacholder. 2002. One gene and one outcome? No way. Trends in Molecular Medicine 8 (6): 266–269.
Cited by
52 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献