Lack of Access to Genetic-Relative Family Health History: A Health Disparity for Adoptees?

American Journal of Bioethics 16 (12):43-45 (2016)
  Copy   BIBTEX

Abstract

This article has no associated abstract. (fix it)

Categories

Keywords

Reprint years

DOI

10.1080/15265161.2016.1240257

Links

PhilArchive



    Upload a copy of this work     Papers currently archived: 92,075

External links

Setup an account with your affiliations in order to access resources via your University's proxy server

Through your library

My notes

Similar books and articles

Issues of “Cost, Capabilities, and Scope” in Characterizing Adoptees' Lack of “Genetic-Relative Family Health History” as an Avoidable Health Disparity: Response to Open Peer Commentaries on “Does Lack of ‘Genetic-Relative Family Health History’ Represent a Potentially Avoidable Health Disparity for Adoptees?”.Thomas May, James P. Evans, Kimberly A. Strong, Kaija L. Zusevics, Arthur R. Derse, Jessica Jeruzal, Alison LaPean Kirschner, Michael H. Farrell & Harold D. Grotevant - 2016 - American Journal of Bioethics 16 (12):4-8.
No Panacea: Next-Gen Sequencing Will Not Mitigate Adoptees’ Lack of Genetic Family Health History.Stephanie M. Fullerton - 2016 - American Journal of Bioethics 16 (12):41-43.
Necessary Health Care and Basic Needs: Health Insurance Plans and Essential Benefits. [REVIEW]Andrew Ward & Pamela Jo Johnson - 2013 - Health Care Analysis 21 (4):355-371.
Social Justice, Health Disparities, and Culture in the Care of the Elderly.Peggye Dilworth-Anderson, Geraldine Pierre & Tandrea S. Hilliard - 2012 - Journal of Law, Medicine and Ethics 40 (1):26-32.
Begging the Question: The Fallacy of Adoptees as a Health Disparity.Gwendolyn P. Quinn & Susan T. Vadaparampil - 2016 - American Journal of Bioethics 16 (12):47-48.
Genetic Knowledge is a Civil Right. Towards a New Model of Health Contract as Social Contract.Hans-Martin Sass - 2010 - Eubios Journal of Asian and International Bioethics 20 (1):2-9.
Who is my neighbor? A communitarian analysis of access to health care for immigrants.Mark G. Kuczewski - 2011 - Theoretical Medicine and Bioethics 32 (5):327-336.
The Hippocratic Bargain and Health Information Technology.Mark A. Rothstein - 2010 - Journal of Law, Medicine and Ethics 38 (1):7-13.
The Notion of health and the morality of genetic intervention.Erik Malmqvist - 2005 - Medicine, Health Care and Philosophy 9 (2):181-192.
How Does Organisational Literacy Impact Access to Health Care for Homeless Individuals?Naomi Rebecca Hughes - 2017 - Health Care Analysis 25 (1):90-106.
‘Medicine’s Next Goldmine?’ The Implications of New Genetic Health Technologies for the Health Service.Michael Calnan, David Wainwright, Peter Glasner, Ruth Newbury-Ecob & Ewan Ferlie - 2005 - Medicine, Health Care and Philosophy 9 (1):33-41.
Reassessing insurers' access to genetic information: Genetic privacy, ignorance, and injustice.Eli Feiring - 2008 - Bioethics 23 (5):300-310.
When Public Health and Genetic Privacy Collide: Positive and Normative Theories Explaining How ACA's Expansion of Corporate Wellness Programs Conflicts with GINA's Privacy Rules.Jennifer S. Bard - 2011 - Journal of Law, Medicine and Ethics 39 (3):469-487.
Well-Being and the Capability of Health.Christopher A. Riddle - 2013 - Topoi 32 (2):153-160.
Ethics and value strategies used in prioritizing mental health services in oregon.David A. Pollack, Bentson H. McFarland, Robert A. George & Richard H. Angell - 1993 - HEC Forum 5 (5):322-339.

Analytics

Added to PP
2016-12-01

Downloads
27 (#590,878)

6 months
10 (#270,763)

Historical graph of downloads
How can I increase my downloads?

Author's Profile

Inmaculada de Melo-Martin
Weill Cornell Medicine--Cornell University

Citations of this work

Add more citations

References found in this work

Add more references