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4. On the future of genomic data. Kahn SD Science; 2011 Feb; 331(6018):728-9. PubMed ID: 21311016 [TBL] [Abstract][Full Text] [Related]
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7. Proxy consent and a national DNA databank: an unethical and discriminatory combination. Baumann TK Iowa Law Rev; 2001 Jan; 86(2):667-701. PubMed ID: 16184651 [No Abstract] [Full Text] [Related]
8. Personal genomes: when consent gets in the way. Taylor P Nature; 2008 Nov; 456(7218):32-3. PubMed ID: 18987719 [No Abstract] [Full Text] [Related]
9. Enabling responsible public genomics. Conley JM; Doerr AK; Vorhaus DB Health Matrix Clevel; 2010; 20(2):325-85. PubMed ID: 21243847 [TBL] [Abstract][Full Text] [Related]
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13. Tribal groups attack ethics of genome diversity project. Macilwain C Nature; 1996 Sep; 383(6597):208. PubMed ID: 8805684 [No Abstract] [Full Text] [Related]
14. Solidarity and justice as guiding principles in genomic research. Hoedemaekers R; Gordijn B; Pijnenburg M Bioethics; 2007 Jul; 21(6):342-50. PubMed ID: 17845458 [TBL] [Abstract][Full Text] [Related]
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