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Genetic Testing, Arribas-Ayllon


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Автор: Arribas-Ayllon
Название:  Genetic Testing
ISBN: 9781138019966
Издательство: Taylor&Francis
Классификация:

ISBN-10: 1138019968
Обложка/Формат: Paperback
Страницы: 224
Вес: 0.36 кг.
Дата издания: 18.02.2014
Серия: Genetics and society
Язык: English
Иллюстрации: 1 line drawings, black and white; 1 halftones, black and white; 2 illustrations, black and white
Размер: 232 x 156 x 13
Читательская аудитория: Undergraduate
Ключевые слова: Sociology, LAW / Science & Technology,MEDICAL / Ethics,MEDICAL / Genetics
Подзаголовок: Accounts of autonomy, responsibility and blame
Ссылка на Издательство: Link
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Поставляется из: Европейский союз
Описание:

Advances in molecular genetics have led to the increasing availability of genetic testing for a variety of inherited disorders. While this new knowledge presents many obvious health benefits to prospective individuals and their families it also raises complex ethical and moral dilemmas for families as well as genetic professionals.

This book explores the ways in which genetic testing generates not only probabilities of potential futures, but also enjoys new forms of social, individual and professional responsibility. Concerns about confidentiality and informed consent involving children, the assessment of competence and maturity, the ability to engage in shared decision-making through acts of disclosure and choice, are just some of the issues that are examined in detail.




Genetic Privacy: An Evaluation Of The Ethical And Legal Landscape

Автор: Kaan Terry Sheung-Hung Et Al
Название: Genetic Privacy: An Evaluation Of The Ethical And Legal Landscape
ISBN: 1783263059 ISBN-13(EAN): 9781783263059
Издательство: World Scientific Publishing
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Цена: 20592.00 р.
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Описание: Privacy is an unwieldy concept that has eluded an essentialised definition despite its centrality and importance in the body of bioethics. The compilation presented in this volume represents continuing discussions on the theme of privacy in the context of genetic information. It is intended to present a wide range of expert opinion in which the notion of privacy is examined from many perspectives, in different contexts and imperatives, and in different societies, with the hope of advancing an understanding of privacy through the examination and critique of some of its evolving component concepts such as notions of what constitute the personal, the context of privacy, the significance and impact of the relational interests of others who may share the same genetic inheritance, and mechanisms for the protection of privacy (as well as of their limitations), among others. More specifically, the discussions in this volume encourages us to think broadly about privacy, as encompassing values that are entailed in the sociality of context and of relations, and also as freedom from illegitimate and excessive surveillance. A long-standing question that continues to challenge us is whether genetic information should be regarded as exceptional, as it is often perceived. A conclusion that could be derived from this volume is that while genetic information may be significant, it is not exceptionally so. The work presented in this volume underlines the continuing and growing relevance of notions of privacy to genomic science, and the need to take ownership of a genetic privacy for the future through broad, rigorous and open discussion.Contributors: Alastair V Campbell, Benjamin Capps, Jacqueline JL Chin, Oi Lian Kon, Kenji Matsui, Thomas H Murray, Nazirudin Mohd Nasir, Dianne Nicol, Anh Tuan Nuyen, Onora O'Neill, Margaret Otlowski, Yvette van der Eijk, Chunshui Wang, Ross S White.

Normative and Pragmatic Dimensions of Genetic Counseling

Автор: Fanning
Название: Normative and Pragmatic Dimensions of Genetic Counseling
ISBN: 3319449281 ISBN-13(EAN): 9783319449289
Издательство: Springer
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Цена: 11878.00 р.
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Описание:

This book provides an elaboration and evaluation of the dominant conceptions of genetic counseling as they are accounted for in three different models: the teaching model; the psychotherapeutic model; and the responsibility model. The elaboration of these models involves an identification of the larger traditions, visions and theories of communication that underwrite them; the evaluation entails an assessment of each model’s theses and ultimately a comparison of their adequacy in response to two important concerns in genetic counseling: the contested values of non-directiveness and the recognition of differences across perspectives, with special focus on how religious and spiritual beliefs of patients are coordinated with the networks of meaning in genetics. Several insights are made explicit in this project through the work of Robert Brandom. Brandom’s deontic scorekeeping model demonstrates how dialogue is at the root of grasping a conceptual content. Against this backdrop, professional communications such as genetic counseling can be seen as late developments in linguistic practices that have structural challenges. Brandom’s model reminds us that the professional needs the client’s understanding to grasp conceptual content in a particular context.
AIDS, Women and the Next Generation Towards a Morally Acceptable Public Policy for HIV Testing of Pregnant Women and Newborns (Hardback)

Автор: Faden, Ruth R.; Geller, Gail; Powers, Madison
Название: AIDS, Women and the Next Generation Towards a Morally Acceptable Public Policy for HIV Testing of Pregnant Women and Newborns (Hardback)
ISBN: 0195065727 ISBN-13(EAN): 9780195065725
Издательство: Oxford Academ
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Цена: 7522.00 р.
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Описание: One of the tragic factors of the AIDS epidemic as it moves into its second decade is the growing number of infected women and children. This is the first scholarly book on AIDS devoted specifically to public policies affecting women and children. It sets in historical perspective a comprehensive analysis of the ethical, legal, clinical, and public health issues raised by a central policy question affecting women and children - whether and under what conditionspregnant women and newborns should be tested for evidence of HIV infection. Written by an interdisciplinary group of national experts, this book examines how these recommendations should change in the future, with advances in testing technologies and therapies.

The Governance of Genetic Information

Автор: Widdows
Название: The Governance of Genetic Information
ISBN: 1107625424 ISBN-13(EAN): 9781107625426
Издательство: Cambridge Academ
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Цена: 5069.00 р.
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Описание: This volume maps the areas of ethical concern in the debate regarding the governance of genetic information, and suggests alternative ethical frameworks and models of regulation in order to inform its restructuring.

Perspectives on Genetic Discrimination

Автор: Lemke
Название: Perspectives on Genetic Discrimination
ISBN: 1138952443 ISBN-13(EAN): 9781138952447
Издательство: Taylor&Francis
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Цена: 6123.00 р.
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Описание: This is the first book to critically evaluate the empirical evidence and the theoretical usefulness of the concept of "genetic discrimination." It discusses the advantages and limitations of adopting the concept, and offers a more complex account distinguishing between several dimensions and forms of genetic discrimination.

Genetic Democracy

Автор: Veikko Launis; Juha R?ikk?
Название: Genetic Democracy
ISBN: 9048175666 ISBN-13(EAN): 9789048175666
Издательство: Springer
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Цена: 27951.00 р.
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Описание: This book provides an in-depth analysis of the ethical, social and philosophical issues related to modern genetic research and gene technology.

Ethical Dilemmas in Genetics and Genetic Counseling

Автор: Berliner, Janice
Название: Ethical Dilemmas in Genetics and Genetic Counseling
ISBN: 019994489X ISBN-13(EAN): 9780199944897
Издательство: Oxford Academ
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Цена: 8395.00 р.
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Описание: Ethical Dilemmas in Genetic Counseling: Principles through Case Scenarios is essential reading for anyone interested in the ethical issues surfacing in common genetics practice. Written exclusively by genetic counselors, it makes a significant contribution to the field of ethics in genetics and thus will appeal not only to genetic counselors but to physicians, nurses, and all those concerned with bioethics and social science.


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