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Your Biobank, Your Doctor?: The right to full disclosure of population biobank findings
The advent of personal genomics companies offering direct translation of scientific data into personal health information, calls into question traditional policies to refuse disclosure of such scientific data to research participants. This seems especially true for population biobanks, as they colle...
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| Publicado no: | Genom Soc Policy |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Springer Berlin Heidelberg
2009
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5425046/ https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1746-5354-5-1-55 |
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