Negotiating Risk : : British Pakistani Experiences of Genetics / / Alison Shaw.
Drawing on fieldwork with British Pakistani clients of a UK genetics service, this book explores the personal and social implications of a ‘genetic diagnosis’. Through case material and comparative discussion, the book identifies practical ethical dilemmas raised by new genetic knowledge and shows h...
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Superior document: | Title is part of eBook package: De Gruyter Berghahn Books Complete eBook-Package 2000-2013 |
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Place / Publishing House: | New York; , Oxford : : Berghahn Books, , [2009] ©2009 |
Year of Publication: | 2009 |
Language: | English |
Online Access: | |
Physical Description: | 1 online resource (320 p.) |
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001 | 9781845458874 | ||
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100 | 1 | |a Shaw, Alison, |e author. |4 aut |4 http://id.loc.gov/vocabulary/relators/aut | |
245 | 1 | 0 | |a Negotiating Risk : |b British Pakistani Experiences of Genetics / |c Alison Shaw. |
264 | 1 | |a New York; |a Oxford : |b Berghahn Books, |c [2009] | |
264 | 4 | |c ©2009 | |
300 | |a 1 online resource (320 p.) | ||
336 | |a text |b txt |2 rdacontent | ||
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338 | |a online resource |b cr |2 rdacarrier | ||
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505 | 0 | 0 | |t Frontmatter -- |t CONTENTS -- |t List of Figures -- |t Acknowledgements -- |t Introduction: Exploring genetic risk -- |t Chapter 1: Medical and public perceptions of consanguineous marriage and genetic risk -- |t Chapter 2: Close kin marriages: some anthropological theory and European history -- |t Chapter 3: British Pakistani cousin marriages: balancing marital risks -- |t Chapter 4: Medical surveillance and diagnostic uncertainty -- |t Chapter 5: Responding to reproductive risk -- |t Chapter 6: Foretelling and managing infant death -- |t Chapter 7: Genetic screening and the extended family -- |t Chapter 8: Genetic risk in context -- |t Bibliography -- |t Index |
506 | 0 | |a restricted access |u http://purl.org/coar/access_right/c_16ec |f online access with authorization |2 star | |
520 | |a Drawing on fieldwork with British Pakistani clients of a UK genetics service, this book explores the personal and social implications of a ‘genetic diagnosis’. Through case material and comparative discussion, the book identifies practical ethical dilemmas raised by new genetic knowledge and shows how, while being shaped by culture, these issues also cross-cut differences of culture, religion and ethnicity. The book also demonstrates how identifying a population-level elevated ‘risk’ of genetic disorders in an ethnic minority population can reinforce existing social divisions and cultural stereotypes. The book addresses questions about the relationship between genetic risk and clinical practice that will be relevant to health workers and policy makers. | ||
538 | |a Mode of access: Internet via World Wide Web. | ||
546 | |a In English. | ||
588 | 0 | |a Description based on online resource; title from PDF title page (publisher's Web site, viewed 07. Nov 2022) | |
650 | 0 | |a Consanguinity. | |
650 | 0 | |a Culture. | |
650 | 0 | |a Medicine. | |
650 | 0 | |a Philosophy. | |
650 | 0 | |a Risk assessment. | |
650 | 7 | |a SOCIAL SCIENCE / Anthropology / General. |2 bisacsh | |
773 | 0 | 8 | |i Title is part of eBook package: |d De Gruyter |t Berghahn Books Complete eBook-Package 2000-2013 |z 9783110998283 |
856 | 4 | 0 | |u https://doi.org/10.1515/9781845458874 |
856 | 4 | 0 | |u https://www.degruyter.com/isbn/9781845458874 |
856 | 4 | 2 | |3 Cover |u https://www.degruyter.com/document/cover/isbn/9781845458874/original |
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