- New
-
Topics
- All Categories
- Metaphysics and Epistemology
- Value Theory
- Science, Logic, and Mathematics
- Science, Logic, and Mathematics
- Logic and Philosophy of Logic
- Philosophy of Biology
- Philosophy of Cognitive Science
- Philosophy of Computing and Information
- Philosophy of Mathematics
- Philosophy of Physical Science
- Philosophy of Social Science
- Philosophy of Probability
- General Philosophy of Science
- Philosophy of Science, Misc
- History of Western Philosophy
- Philosophical Traditions
- Philosophy, Misc
- Other Academic Areas
- Journals
- Submit material
- More
Attitudes of physicians and patients towards disclosure of genetic information to spouse and first-degree relatives: a case study from Turkey
BMC Medical Ethics 15 (1):39 (2014)
Abstract
When considering the principle of medical confidentiality, disclosure of genetic information constitutes a special case because of the impact that this information can have on the health and the lives of relatives. The aim of this study is to explore the attitudes of Turkish physicians and patients about sharing information obtained from genetic testsLinks
PhilArchive
External links
(no proxy)
Setup an account with your affiliations in order to access resources via your University's proxy server
Through your library
- Sign in / register and customize your OpenURL resolver
- Configure custom resolver
My notes
Similar books and articles
Disclosure 'downunder': misadventures in Australian genetic privacy law.B. Arnold & W. Bonython - 2014 - Journal of Medical Ethics 40 (3):168-172.
Physicians' Attitudes toward Disclosure of Genetic Information to Third Parties.Gail Geller, Ellen S. Tambor, Barbara A. Bernhardt, Gary A. Chase, Karen J. Hofman, Ruth R. Faden & Neil A. Holtzman - 1993 - Journal of Law, Medicine and Ethics 21 (2):238-240.
Physicians' Attitudes toward Disclosure of Genetic Information to Third Parties.Gail Geller, Ellen S. Tambor, Barbara A. Bernhardt, Gary A. Chase, Karen J. Hofman, Ruth R. Faden & Neil A. Holtzman - 1993 - Journal of Law, Medicine and Ethics 21 (2):238-240.
Israeli Nurses and Genetic Information Disclosure.Sivia Barnoy & Nili Tabak - 2007 - Nursing Ethics 14 (3):280-294.
Who Are You Going to Call? Primary Care Patients’ Disclosure Decisions Regarding Direct–to–Consumer Genetic Testing.Katherine Wasson, Sara Cherny, Tonya Nashay Sanders, Nancy S. Hogan & Kathy J. Helzlsouer - 2014 - Narrative Inquiry in Bioethics 4 (1):53-68.
Facing legal barriers regarding disclosure of genetic information to relatives.Roy Gilbar & Sivia Barnoy - 2020 - New Genetics and Society 39 (4):483-501.
The Right Not to Know and the Duty to Tell: The Case of Relatives.Niklas Juth - 2014 - Journal of Law, Medicine and Ethics 42 (1):38-52.
Familial disclosure by genetic healthcare professionals: a useful but sparingly used legal provision in France.Benjamin Derbez, Antoine de Pauw, Dominique Stoppa-Lyonnet, Frédéric Galactéros & Sandrine de Montgolfier - 2019 - Journal of Medical Ethics 45 (12):811-816.
Analytics
Added to PP
2014-05-16
Downloads
30 (#520,442)
6 months
6 (#700,231)
2014-05-16
Downloads
30 (#520,442)
6 months
6 (#700,231)
Historical graph of downloads
Citations of this work
‘Is this knowledge mine and nobody else's? I don't feel that.’ Patient views about consent, confidentiality and information-sharing in genetic medicine: Table 1.Sandi Dheensa, Angela Fenwick & Anneke Lucassen - 2016 - Journal of Medical Ethics 42 (3):174-179.
From proband to provider: is there an obligation to inform genetic relatives of actionable risks discovered through direct-to-consumer genetic testing?Jordan A. Parsons & Philip E. Baker - 2022 - Journal of Medical Ethics 48 (3):205-212.
How do healthcare professionals respond to ethical challenges regarding information management? A review of empirical studies.Cornelius Ewuoso, Susan Hall & Kris Dierickx - 2021 - Global Bioethics 32 (1):67-84.
Respectful care of human dignity: how is it perceived by patients and nurses?Rahime Aydın Er, Aysel İncedere & Selda Öztürk - 2018 - Journal of Medical Ethics 44 (10):675-680.
The Concept of “Genetic Responsibility” and Its Meanings: A Systematic Review of Qualitative Medical Sociology Literature.Jon Leefmann, Manuel Schaper & Silke Schicktanz - 2017 - Frontiers in Sociology 18 (1):1-22.
References found in this work
Principles of biomedical ethics.Tom L. Beauchamp - 1979 - New York: Oxford University Press. Edited by James F. Childress.
Principles of Biomedical Ethics.Ezekiel J. Emanuel, Tom L. Beauchamp & James F. Childress - 1995 - Hastings Center Report 25 (4):37.
Clinical ethics: a practical approach to ethical decisions in clinical medicine.Albert R. Jonsen, Mark Siegler & William J. Winslade - 2015 - New York: McGraw-Hill Education. Edited by Mark Siegler & William J. Winslade.
Resolving ethical dilemmas: a guide for clinicians.Bernard Lo - 1994 - Baltimore: Williams & Wilkins.
Clinical Ethics: A Practical Approach to Ethical Decisions in Clinical Medicine.Henry Aranow, Albert R. Jonsen, Mark Siegler & William J. Winslade - 1983 - Hastings Center Report 13 (1):32.
PhilPapers logo by Andrea Andrews and Meghan Driscoll.
This site uses cookies and Google Analytics (see our terms & conditions for details regarding the privacy implications). Use of this site is subject to terms & conditions.
All rights reserved by The PhilPapers Foundation
Server: philpapers-web-6686886f5-5pqs9 uwo