| scholarly article | Q13442814 |
| P356 | DOI | 10.1159/000336861 |
| P698 | PubMed publication ID | 22722692 |
| P2093 | author name string | J Ried | |
| A Bialobrzeski | |||
| P Dabrock | |||
| P2860 | cites work | From genetic privacy to open consent | Q24550752 |
| DNA databanks and consent: a suggested policy option involving an authorization model | Q24795476 | ||
| Human genetic research, DNA banking and consent: a question of 'form'? | Q30664023 | ||
| Coding and consent: moral challenges of the database project in Iceland. | Q34323542 | ||
| Broadening consent--and diluting ethics? | Q34933645 | ||
| Human genetic research: emerging trends in ethics | Q35998786 | ||
| Changing perspectives in biobank research: from individual rights to concerns about public health regarding the return of results | Q39976746 | ||
| Free riders and pious sons--why science research remains obligatory | Q42220716 | ||
| Hippocrates revisited? Old ideals and new realities | Q42403914 | ||
| Of genomics and public health: Building public "goods"? | Q42636949 | ||
| Genomic databases as global public goods? | Q45951382 | ||
| The communitarian turn: myth or reality? | Q48611579 | ||
| Does an appeal to the common good justify individual sacrifices for genomic research? | Q53222505 | ||
| Solidarity and equity: new ethical frameworks for genetic databases | Q56815400 | ||
| P433 | issue | 5 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | informed consent | Q764527 |
| public good | Q272458 | ||
| P304 | page(s) | 285-292 | |
| P577 | publication date | 2012-06-20 | |
| P1433 | published in | Public Health Genomics | Q15766289 |
| P1476 | title | Differentiating and evaluating common good and public good: making implicit assumptions explicit in the contexts of consent and duty to participate. | |
| P478 | volume | 15 |
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