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Virtual Mentor. September 2009, Volume 11, Number 9: 649-743. Full Issue PDF September 2009 ContentsEthical Questions in Genetic TestingEthics PollFrom the Editor in ChiefIf You Build It From the EditorExamining the Benefits and Harms of Genetic Information Educating for ProfessionalismClinical CasesDuty to Warn At-Risk Family Members of Genetic Disease Presymptomatic Testing of Children for Huntington’s Disease Evaluating Requests for Preimplantation Genetic Diagnosis Medical EducationWhat Is the Role of Nongeneticist Physicians, and Are They Prepared for It? The Code SaysAMA Code of Medical Ethics’ Opinions on Genetic Testing Journal DiscussionConscientious Objection: A Medical Student Perspective Clinical PearlCapturing the Power of the Family History Law, Policy, and SocietyHealth LawA Physician’s Duty to Warn Third Parties of Hereditary Risk Policy ForumDirect-to-Consumer Personal Genome Services: Need for More Oversight Emerging Dilemmas in Newborn Screening Medicine and SocietyGetting Personal with DNA: From Genome to Me-Ome Op-Ed and CorrespondenceOp-EdInformed Consent and Prenatal Testing: The Kennedy-Brownback Act Unethical Protection of Conscience: Defending the Powerful against the Weak ResourcesSuggested Readings and Resources About the Contributors © 2009 American Medical Association. All Rights Reserved. |