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Consent in genomic research in malaria (MalariaGEN)
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The concept of social value in developing countries
The impact of genetic risk in UK Pakistani families
The use of patient records in e-science research in medicine
MalariaGEN overview
Ethical challenges in the release and publication of ethnicity-related research results (MalariaGEN)
The roles of ethics in effective global genomics research networks (MalariaGEN)
Consent in genomic research in malaria (MalariaGEN)
Ethics of research from the perspective of developing countries-Pakistan as a case study
Strengthening ethical practice in population-based genetics and genomics research: participant views arising from Sickle-Cell Disease screening activities in East Africa
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