| scholarly article | Q13442814 |
| P2093 | author name string | Rhodes R | |
| P433 | issue | 1 | |
| P304 | page(s) | 10-30 | |
| P577 | publication date | 1998-02-01 | |
| P1433 | published in | Journal of Medicine and Philosophy | Q15756915 |
| P1476 | title | Genetic links, family ties, and social bonds: rights and responsibilities in the face of genetic knowledge. | |
| P478 | volume | 23 |
| Q48524286 | "Please don't tell me". The right not to know |
| Q34504632 | Antenatal genetic testing and the right to remain in ignorance |
| Q48084788 | Autonomy, the Right Not to Know, and the Right to Know Personal Research Results: What Rights Are There, and Who Should Decide about Exceptions? |
| Q35557192 | Can Broad Consent be Informed Consent? |
| Q96133689 | Commentary: In Search of Medical Ethics and Its Foundation with Rosamond Rhodes |
| Q42651452 | Communicating genetic information in the family: enriching the debate through the notion of integrity |
| Q36776962 | Concepts of "person" and "liberty," and their implications to our fading notions of autonomy |
| Q48037860 | Consent to epistemic interventions: a contribution to the debate on the right (not) to know. |
| Q88053926 | Developing Shared Appraisals of Diabetes Risk Through Family Health History Feedback: The Case of Mexican-Heritage Families |
| Q41039435 | Different concepts and models of information for family-relevant genetic findings: comparison and ethical analysis |
| Q37420643 | Diversity and uniformity in genetic responsibility: moral attitudes of patients, relatives and lay people in Germany and Israel |
| Q35893384 | Ethical implications in genetic counseling and family studies of the epilepsies |
| Q34420838 | Ethical implications of genetic testing for breast cancer susceptibility |
| Q39927556 | Ethical, legal and social implications of prenatal and preimplantation genetic testing for cancer susceptibility |
| Q58668566 | Ethics, policy, and rare genetic disorders: the case of Gaucher disease in Israel |
| Q58040158 | FURTHERING INJUSTICES AGAINST WOMEN: GENETIC INFORMATION, MORAL OBLIGATIONS, AND GENDER |
| Q39292307 | Families' experience of oncogenetic counselling: accounts from a heterogeneous hereditary cancer risk population |
| Q24681950 | Firing up the nature/nurture controversy: bioethics and genetic determinism |
| Q56764682 | Free Choice and Patient Best Interests |
| Q92195938 | Genetic Moralism and Health |
| Q38119935 | Genetic counselling in ALS: facts, uncertainties and clinical suggestions |
| Q56906011 | Genetic ignorance and reasonable paternalism |
| Q34504617 | Genetic information, rights, and autonomy |
| Q36687387 | Genetic privacy: orthodoxy or oxymoron? |
| Q45077765 | Genetic professionals' reports of nondisclosure of genetic risk information within families |
| Q44229289 | Genetic testing of children for familial cancers: a comparative legal perspective on consent, communication of information and confidentiality |
| Q24658487 | Genomic knowledge sharing: A review of the ethical and legal issues |
| Q36417821 | Guidelines for disclosing genetic information to family members: from development to use. |
| Q35998786 | Human genetic research: emerging trends in ethics |
| Q30363555 | Immanuel Kant, his philosophy and medicine. |
| Q34504638 | Just ignore it? Parents and genetic information |
| Q57911018 | Limited Relevance of the Right Not to Know—Reflections on a Screening Study |
| Q35825826 | Looking for Trouble: Preventive Genomic Sequencing in the General Population and the Role of Patient Choice |
| Q37169821 | Point-counterpoint. Ethics and genomic incidental findings |
| Q57266076 | Policy recommendations for carrier testing and predictive testing in childhood: a distinction that makes a real difference |
| Q24682050 | Prescribing cannabis: freedom, autonomy, and values |
| Q57768923 | Questioning the consensus: managing carrier status results generated by newborn screening |
| Q53756850 | Resisting Paternalism in Prenatal Whole-Genome Sequencing. |
| Q48017275 | Scrutinizing the Right Not to Know |
| Q47558303 | The Ethics of General Population Preventive Genomic Sequencing: Rights and Social Justice |
| Q47220681 | The quest for the perfect baby: why do Israeli women seek prenatal genetic testing? |
| Q37321708 | The relative importance of undesirable truths |
Search more.