The New Genetics: From Research into Health Care Social and Ethical Implications for Users and Providers
ciples and recommendations on genetic service provision in a multidisciplinary way. At the workshop the main issues and principles that are presently emerging as integral parts of national and international recommendations on genetic service provision such as: - voluntary provision of services - pro...
| Other Authors: | , , |
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| Format: | eBook |
| Language: | English |
| Published: |
Berlin, Heidelberg
Springer Berlin Heidelberg
1999, 1999
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| Edition: | 1st ed. 1999 |
| Subjects: | |
| Online Access: | |
| Collection: | Springer Book Archives -2004 - Collection details see MPG.ReNa |
Table of Contents:
- Introduction: The New Genetics: Social and EthicalFrom Research into Health Care — Implications for Users and Providers.
- Opening Address
- Session I: The Provision of the New Genetics: In Whose Best Interest?
- Americans’ Attitudes toward Informed Consent for Breast Cancer Susceptibility Testing: Questions for Cross-Cultural Research
- Nondirectiveness — Facts, Fiction, and Future Prospects
- Predictive Genetic Tests: Destiny or Danger?
- Session II: Providing the New Genetics in Primary Care: Problems and Perspectives
- Genetic Services in Europe — Primary Care Genetics Is a Priority for Health Care Systems
- Education in Genetics
- Genesis, Compulsions, Acceptability, and Future of Pre-Natal Sex-Selection in India
- Session III: Can the Implementation of New Genetic Tests Be Safeguarded by Consensus Policy Recommendations?
- Ethics and Genetics in International Perspective: Results of a Survey
- Consensus and Variation among Medical Geneticists and Patients on the Provision of the New Genetics in Germany — Data from the 1994-1996 Survey among Medical Geneticists and Patients
- The Case for Proposed International Guidelines on Ethical Issues in Medical Genetics
- Session IV: Critiques on the Provision of the New Genetics: Pros and Cons from Consumer and Provider Perspectives
- Statement on CF-Heterozygote Testing
- The Patients’ Perspective on the Provision of Genetic Testing
- The European Alliance of Genetic Support Groups, Their Ethical Code and the Provision of Genetic Services
- What Could a Balance Look Like between Individual Autonomy and Society’s Need to Regulate?
- New Genetics, New Ethics?
- Guidelines on Ethical Issues in Medical Genetics and the Provision of Genetic Services