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The Hastings Center Report explores the ethical, legal, and social issues in medicine, health care, public health, and the life sciences. Six issues are published each year, containing an assortment of essays, columns on legal and policy developments, case studies of issues in clinical care and institutional administration, caregivers' stories, peer-reviewed scholarly articles, and book reviews. Authors come from an assortment of professions and academic disciplines and bring a range of perspectives and political opinions. We welcome submissions from new authors. The Report's readership includes physicians, nurses, scholars of many stripes, administrators, social workers, health lawyers, and others.

Publisher: The Hastings Center

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July-August 2005

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Field Notes

field notes
pp. 1-1(1)
Author: Maschke, Karen

From the Editor

Making Policy
pp. 2-2(1)

Another Voice

How Not to Think about Genetic Information
pp. 3-3(1)
Author: Manson, Neil C.

Letters

In Brief

The Afterlife of Terri Schiavo
pp. 8-8(1)
Authors: Fins, Joseph J.; Schiff, Nicholas D.

In Practice

Not at Peace
pp. 9-10(2)
Author: Bernacki, Rachelle

In Memoriam

In Memoriam: Marc Lappé
pp. 10-11(2)
Author: Callahan, Daniel

At Law

A Government of Limited Powers
pp. 11-12(2)
Author: Schneider, Carl E.

Policy & Politics

Realbioethik
pp. 13-14(2)
Author: Charo, R. Alta

Case Study

Before He Wakes
pp. 15-16(2)
Authors: Lindemann, Hilde; Callahan, Daniel

Essays

Doctors of Interrogation
pp. 17-22(6)
Author: Marks, Jonathan H.

Bioethics Matures: The Field Faces the Future
pp. 22-24(3)
Authors: Wolf, Susan M.; Kahn, Jeffrey P.

Alternative Sources for Stem Cells
pp. 24-26(3)
Author: Steinbock, Bonnie

Articles

Genetic Exceptionalism and Legislative Pragmatism
pp. 27-33(7)
Author: Rothstein, Mark A.

Contributors

Contributors
pp. 48-48(1)

Perspective

The Risks of Race in Addressing Health Disparities
pp. 49-49(1)
Author: Craddock Lee, Simon J.

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