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03111nam a22003735i 4500 |
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978-3-642-58486-2 |
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20191027022237.0 |
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cr nn 008mamaa |
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121227s1999 gw | s |||| 0|eng d |
| 020 |
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|a 9783642584862
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| 024 |
7 |
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|a 10.1007/978-3-642-58486-2
|2 doi
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| 040 |
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|a Sistema de Bibliotecas del Tecnológico de Costa Rica
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| 245 |
1 |
4 |
|a The New Genetics: From Research into Health Care
|b Social and Ethical Implications for Users and Providers /
|c edited by Irmgard Nippert, Heidemarie Neitzel, Gerhard Wolff.
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| 250 |
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|a 1st ed. 1999.
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| 260 |
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|a Berlin, Heidelberg :
|b Springer Berlin Heidelberg :
|b Imprint: Springer,
|c 1999.
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| 300 |
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|a X, 169 p. 13 illus.
|b online resource.
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| 336 |
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|a text
|b txt
|2 rdacontent
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| 337 |
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|a computer
|b c
|2 rdamedia
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| 338 |
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|a online resource
|b cr
|2 rdacarrier
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|a 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.
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| 650 |
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|a Human genetics.
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| 650 |
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0 |
|a Medical ethics.
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| 650 |
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0 |
|a Anthropology.
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| 650 |
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0 |
|a Molecular biology.
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| 650 |
1 |
4 |
|a Human Genetics.
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| 650 |
2 |
4 |
|a Theory of Medicine/Bioethics.
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| 650 |
2 |
4 |
|a Anthropology.
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| 650 |
2 |
4 |
|a Molecular Medicine.
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| 700 |
1 |
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|a Nippert, Irmgard.
|e editor.
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| 700 |
1 |
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|a Neitzel, Heidemarie.
|e editor.
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| 700 |
1 |
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|a Wolff, Gerhard.
|e editor.
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| 710 |
2 |
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|a SpringerLink (Online service)
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| 773 |
0 |
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|t Springer eBooks
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| 856 |
4 |
0 |
|u https://doi.org/10.1007/978-3-642-58486-2
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