Abstract
In this chapter, only diagnostic screening for individual patients is considered; and that at any stage from the polar body onwards. Notice is taken of new diagnostic techniques which disclose function as well as genetic composition and structure. Screening is widely accepted, and provision for it is increasing, if slowly. Ethics implies choice: primarily choice by the patient based on the information which it is a clinical duty to provide. Choice is complicated by inherent uncertainty. It is not unlimited: it must be within the law and consistent with professional obligation.
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References
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© 1995 The Galton Institute
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Dunstan, G.R. (1995). ‘Calming or Harming?’ The Ethics of Screening for Fetal Defects. In: Barron, S.L., Roberts, D.F. (eds) Issues in Fetal Medicine. Studies in Biology, Economy and Society. Palgrave Macmillan, London. https://doi.org/10.1007/978-1-349-23812-5_10
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DOI: https://doi.org/10.1007/978-1-349-23812-5_10
Publisher Name: Palgrave Macmillan, London
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Online ISBN: 978-1-349-23812-5
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