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Human Experimentation Therapeutic Human Experimentation Nontherapeutic Human Experimentation Patient Selection Clinical Trials as Topic Research Design Questionnaires Tissue Conditioning (Dental)Randomized Controlled Trials as Topic Prospective Studies AIDS Serodiagnosis Control Groups Risk Assessment Sensitivity and Specificity Pilot Projects Records as Topic Reproducibility of Results Surgical Procedures, Operative Clinical Trials, Phase I as Topic Surgical Procedures, Elective Clinical Trials, Phase IV as Topic Treatment Outcome Embryo Disposition Medical Records Cross-Sectional Studies Data Collection Genetic Testing Focus Groups Models, Molecular Interviews as Topic Feasibility Studies Magnetic Resonance Imaging Image Interpretation, Computer-Assisted Polymerase Chain Reaction Donor Selection Risk Factors Mass Screening

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Templates, Genetic Base Sequence Transcription, Genetic DNA Replication Sensitivity and Specificity Time Factors Nucleic Acid Conformation DNA, Single-Stranded Pregnancy Kinetics Mutation Algorithms

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Human Experimentation Therapeutic Human Experimentation Nontherapeutic Human Experimentation Biomedical Research Genetic Research Research Design Emergency Medicine General Surgery Empirical Research Research Anesthesiology Qualitative Research

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Informed Consent Consent Forms Presumed Consent Parental Consent Mental Competency Third-Party Consent Disclosure Personal Autonomy Confidentiality Patient Rights Informed Consent By Minors Patient Advocacy Patient Education as Topic Truth Disclosure Privacy Child Advocacy Duty to Warn Government Regulation Liability, Legal Treatment Refusal Malpractice Public Opinion Health Literacy Jurisprudence Therapeutic Misconception Genetic Privacy Defensive Medicine Internationality Human Rights Judicial Role Freedom Parents United States Office of Research Integrity Compensation and Redress War Crimes Access to Information Federal Government Family Cultural Diversity Physician Impairment Social Justice Duty to Recontact

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Ethics, Research Personal Autonomy Ethics, Medical Beneficence Ethics Committees, Research Ethics, Clinical Bioethical Issues Helsinki Declaration Conflict of Interest Ethical Review Ethics Committees Morals Moral Obligations Bioethics Therapeutic Misconception Codes of Ethics Ethics, Professional Therapeutic Equipoise Ethics Principle-Based Ethics Social Responsibility Social Justice

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Disclosure Questionnaires Communication Base Sequence Documentation Molecular Sequence Data Health Literacy Audiovisual Aids Multimedia Records as Topic Information Dissemination Medical Records Access to Information Data Collection Focus Groups Interviews as Topic Image Interpretation, Computer-Assisted Pamphlets Communication Barriers Journalism, Medical Algorithms Editorial Policies

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Informed Consent Consent Forms Presumed Consent Parental Consent Mental Competency Third-Party Consent Ethics, Research Personal Autonomy Ethics, Medical Ethics Committees, Research Biological Specimen Banks Confidentiality Patient Rights Informed Consent By Minors Patient Advocacy Ethics, Clinical Patient Selection Clinical Trials as Topic Patient Participation Patient Education as Topic Physician-Patient Relations Privacy Child Advocacy Helsinki Declaration Conflict of Interest Ethical Review Questionnaires Duty to Warn Ethics Committees Government Regulation Liability, Legal Professional Staff Committees Tissue and Organ Procurement Treatment Refusal Randomized Controlled Trials as Topic Prospective Studies Malpractice Voluntary Programs Bioethics Health Literacy Jurisprudence Codes of Ethics Ethics, Professional Ethics Genetic Privacy Defensive Medicine Guidelines as Topic Risk Assessment Sensitivity and Specificity Selection Bias Human Rights Pilot Projects Patient Satisfaction Attitude to Health Records as Topic Reproducibility of Results Freedom Clinical Trials, Phase I as Topic United States Office of Research Integrity Clinical Trials, Phase IV as Topic Patient Identification Systems Treatment Outcome Compensation and Redress Medical Records Cross-Sectional Studies Data Collection Practice Guidelines as Topic Genetic Testing Forms and Records Control Focus Groups Institute of Medicine (U.S.)Interviews as Topic Federal Government Feasibility Studies Legislation, Medical Educational Status Clinical Trials Data Monitoring Committees Physician Impairment Consumer Participation Hospitals, Teaching Donor Selection Emergencies Risk Factors Mass Screening Social Justice Duty to Recontact

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Clinical Trial, Phase III

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Informed Consent Consent Forms Templates, Genetic Presumed Consent Parental Consent Mental Competency Research Subjects Third-Party Consent Human Experimentation Disclosure Ethics, Research Therapeutic Human Experimentation Nontherapeutic Human Experimentation Comprehension Personal Autonomy Ethics, Medical Beneficence Minors Ethics Committees, Research Biological Specimen Banks Biomedical Research Genetic Research Refusal to Participate Confidentiality Patient Rights Informed Consent By Minors Paternalism Patient Advocacy Ethics, Clinical Decision Making Patient Selection Legal Guardians Clinical Trials as Topic Patient Participation Researcher-Subject Relations Bioethical Issues Patient Education as Topic Truth Disclosure Physician-Patient Relations Privacy Child Advocacy Helsinki Declaration Conflict of Interest Research Design Ethical Review Questionnaires Duty to Warn Ethics Committees Communication Government Regulation Liability, Legal Professional Staff Committees Tissue and Organ Procurement Tissue Conditioning (Dental)Morals Research Personnel Treatment Refusal Moral Obligations Persons Vulnerable Populations Base Sequence Documentation Randomized Controlled Trials as Topic United States Prospective Studies Molecular Sequence Data Malpractice Public Opinion Voluntary Programs Bioethics Health Literacy DNA-Directed RNA Polymerases Jurisprudence Therapeutic Misconception Audiovisual Aids Transcription, Genetic AIDS Serodiagnosis Codes of Ethics DNA-Directed DNA Polymerase Ethics, Professional DNA Replication Therapeutic Equipoise Trust Ethics Genetic Privacy Mentally Ill Persons Control Groups Defensive Medicine Multimedia Guidelines as Topic Risk Assessment Sensitivity and Specificity DNA Great Britain Internationality Principle-Based Ethics Selection Bias Human Rights Social Responsibility Patients

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