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Kansas State Statute (Kansas: KSA §§40-2209, 40-2209p, 40-2257, and 40-2259 )
The statutes restrict the use of genetic tests, information about whether an individual or family member has obtained a genetic test, and test results by a health insurance company, health…- state statute
- Kansas
- health insurance nondiscrimination
- disability
- health maintenance organization
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Additional Resource
North Carolina State Statute (North Carolina: NCGA §§58-3-215, 58-51-45, 58-51-95, 58-65-70, 58-68-30 and 58-…)
A health benefit plan, health maintenance organization or multiple employer welfare arrangement may not raise the premium or contribution rates paid for a group health benefit plan, refuse to issue…- state statute
- North Carolina
- health insurance nondiscrimination
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Publication
Pure selection: The ethics of preimplantation genetic diagnosis and choosing children without abortion
Acta Universitatis GothoburgensisDigital 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
Testimony on embryo research and related issues
National Catholic Bioethics QuarterlyDigital 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
Clinical trials, genetic add-ons, and the question of benefit- sharing
LancetDigital 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
Harmonizing the international regulation of embryonic stem cell research: Possibilities, promises and potential pitfalls
Medical Law InternationalDigital 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
Protecting egg donors and human embryos -- the failure of the South Korean Bioethics and Biosafety Act
Pacific Rim Law and Policy 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
Alternative consent models for biobanks: The new Spanish law on biomedical research
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… -
Publication
Advancing civil rights, the next generation: The Genetic Information Nondiscrimination Act of 2008 and beyond
Health MatrixDigital 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… -
Grant Abstract
Building the Medical Information Commons: Participant Engagement and Policy
Many national and international public and private initiatives are forming to collect and share data on a large scale for research and clinical use. Collectively, these efforts may lead to the…- Affect
- Clinical
- clinical application
- Data
- data sharing