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Publication
Cultural competence and informed consent in international health research
Camb Q Healthc Ethics -
Publication
Ethical implications of including children in a large biobank for genetic-epidemiologic research: A qualitative study of public opinion
Am J Med Genet C Semin Med Genet -
Publication
Perceived quality of life in mothers of children with fragile X syndrome
Am J Ment Retard -
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Publication
Waiving informed consent in newborn screening research: Balancing social value and respect
Am J Genet C Semin Med Genet -
Publication
Fear of health insurance loss among individuals at risk for Huntington disease
Am J Med Genet -
Publication
Public expectations for return of results from large-cohort genetic research
American Journal of BioethicsDigital citation created by the Bioethics Research Library, Georgetown University, for the National Information Resource on Ethics and Human Genetics, a project funded by the United States National… -