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Consent Preferences of UK Research Volunteers for Genetic and Clinical Studies Survey
This survey assesses views on aspects of the consent process, including willingness to share medical information and DNA for different research purposes, including controversial areas of research. -
Publication
Strategies and clinical outcome of 250 cycles of preimplantation genetic diagnosis for single gene disorders
Human ReproductionDigital 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… -
Publication
The most personal information of all: An appraisal of genetic privacy in the shadow of the Human Genome Project
International Journal of Law, Policy and the FamilyDigital 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… -
Publication
Two models for human genetics: Blood grouping and psychiatry in Germany between the World Wars
Bulletin of the History of MedicineDigital 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… -
Publication
Differences between African Americans and whites in their attitudes toward genetic testing for Alzheimer's disease
Genetic TestingDigital 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… -
Publication
The right to remain in ignorance about genetic information--can such a right be defended in the name of autonomy?
New Zealand Medical JournalDigital 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… -
Publication
Hereditary breast/ovarian and colorectal cancer genetics knowledge in a national sample of US physicians
Journal of Medical GeneticsDigital 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… -
Publication
Additional protocol to the Convention on Human Rights and Biomedicine, concerning genetic testing for health purposes
European Journal of Health LawDigital 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… -
Publication
The interface between assisted reproductive technologies and genetics: Technical, social, ethical, and legal issues
European Journal of Human GeneticsDigital 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… -
Publication
Barriers to participating in genetic counseling and BRCA testing during primary treatment for breast cancer
Genetics in MedicineDigital 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…