
Provides the background information every parent needs in order to understand the issues, and to make informed choices, about genetic screening. Describes how the change in policy to include screening for untreatable as well as treatable diseases came about. Provides basic information about the techniques of screening, the practical and ethical choices parents must face, and the public policies behind those choices.
NOTE: NO FURTHER DISCOUNTS FOR ALREADY REDUCED SALE ITEMS.
Target audience are medical practitioners, researchers, and groups dedicated to studying genetic screening and ethical parenting choices, as well as parents interested in genetic screening and how to consider making ethical choices and with what professionals they should consult.
Product Details
- Changing Moral Focus of Newborn Screening
- Ethical Analysis by the President's Council on Bioethics
- Medical screening, Moral and ethical aspects
- Newborn infants, Medical examinations, Moral and ethical aspects