Differences in preferences for models of consent for biobanks between Black and White women
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Public Health, Environmental and Occupational Health,Epidemiology
Link
http://link.springer.com/content/pdf/10.1007/s12687-015-0248-y.pdf
Reference45 articles.
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2. Brothers KB, Morrison DR, Clayton EW (2011) Two large‐scale surveys on community attitudes toward an opt‐out biobank American. Am J Med Genet A 155:2982–2990
3. Chen DT, Rosenstein DL, Muthappan P, Hilsenbeck SG, Miller FG, Emanuel EJ, Wendler D (2005) Research with stored biological samples: what do research participants want? Arch Intern Med 165:652–655
4. Davey Smith G, Ebrahim S, Lewis S, Hansell A, Palmer L, Burton P (2005) Genetic epidemiology and public health: hope, hype, and future prospects. Lancet 366:1484–1498
5. Greely HT (2007) The uneasy ethical and legal underpinnings of large-scale genomic biobanks. Annual Rev Genomics Hum Genet 8:343–364
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