The Journal of Law, Medicine & Ethics

Cover image for The Journal of Law, Medicine & Ethics

December 1995

Volume 23, Issue 4

Pages i–i, 309–410

  1. Contributors

    1. Top of page
    2. Contributors
    3. Recent Developments in Health Law
    1. Contributors (page i)

      Version of Record online: 5 JUN 2007 | DOI: 10.1111/j.1748-720X.1995.tb01371.x

    1. Introduction: The Genome Imperative (pages 309–311)

      Thomas H. Murray and Norman T. Mendel

      Version of Record online: 5 JUN 2007 | DOI: 10.1111/j.1748-720X.1995.tb01372.x

    2. Genetic Information and Health Insurance: State Legislative Approaches (pages 312–319)

      Karen H. Rothenberg

      Version of Record online: 5 JUN 2007 | DOI: 10.1111/j.1748-720X.1995.tb01373.x

    3. Genetic Privacy (pages 320–330)

      Lawrence O. Gostin

      Version of Record online: 5 JUN 2007 | DOI: 10.1111/j.1748-720X.1995.tb01374.x

    4. Testing Children for Genetic Predispositions: Is it in Their Best Interest? (pages 331–344)

      Diane E. Hoffmann and Eric A. Wulfsberg

      Version of Record online: 5 JUN 2007 | DOI: 10.1111/j.1748-720X.1995.tb01375.x

    5. Beyond “Genetic Discrimination”: Toward the Broader Harm of Geneticism (pages 345–353)

      Susan M. Wolf

      Version of Record online: 5 JUN 2007 | DOI: 10.1111/j.1748-720X.1995.tb01376.x

    6. Conflicts in the Biotechnology Industry (pages 354–359)

      Henry T. Greely

      Version of Record online: 5 JUN 2007 | DOI: 10.1111/j.1748-720X.1995.tb01377.x

    7. Drafting the Genetic Privacy Act: Science, Policy, and Practical Considerations (pages 360–366)

      George J. Annas, Leonard H. Glantz and Patricia A. Roche

      Version of Record online: 5 JUN 2007 | DOI: 10.1111/j.1748-720X.1995.tb01378.x

    8. Panel Comment: The Attempt to Pass the Genetic Privacy Act in Maryland (pages 367–370)

      Neil A. Holtzman

      Version of Record online: 5 JUN 2007 | DOI: 10.1111/j.1748-720X.1995.tb01379.x

    9. Panel Comment: Legislating Privacy: The HIV Experience (pages 371–374)

      Wendy E. Parmet

      Version of Record online: 5 JUN 2007 | DOI: 10.1111/j.1748-720X.1995.tb01380.x

    10. Panel Comment: Why the Use of Anonymous Samples for Research Matters (pages 375–377)

      Ellen Wright Clayton

      Version of Record online: 5 JUN 2007 | DOI: 10.1111/j.1748-720X.1995.tb01381.x

    11. Panel Comment: The Impact of the Genetic Privacy Act on Medicine (pages 378–381)

      Philip R. Reilly

      Version of Record online: 5 JUN 2007 | DOI: 10.1111/j.1748-720X.1995.tb01382.x

    12. Ethical Issues Raised by Needle Exchange Programs (pages 382–388)

      Sana Loue, Peter Lurie and Linda S. Lloyd

      Version of Record online: 5 JUN 2007 | DOI: 10.1111/j.1748-720X.1995.tb01383.x

    13. Stemming the Tide: Assisted Suicide and the Constitution (pages 389–397)

      Carl H. Coleman and Tracy E. Miller

      Version of Record online: 5 JUN 2007 | DOI: 10.1111/j.1748-720X.1995.tb01384.x

    14. Ethics Consultation: Anencephaly and Organ Donation (pages 398–400)

      James E. Reagan

      Version of Record online: 5 JUN 2007 | DOI: 10.1111/j.1748-720X.1995.tb01385.x

  2. Recent Developments in Health Law

    1. Top of page
    2. Contributors
    3. Recent Developments in Health Law
    1. Recent Developments in Health Law (pages 403–410)

      Version of Record online: 5 JUN 2007 | DOI: 10.1111/j.1748-720X.1995.tb01387.x

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