<?xml version="1.0" encoding="UTF-8"?><xml><records><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><rec-number>1976</rec-number><ref-type>Audiovisual</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Gert, Bernard</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Who Gets to Know? Genetics and Privacy</style></title></titles><taxonomies><taxonomy><style  face="normal" font="default" size="100%">Science </style></taxonomy><taxonomy><style  face="normal" font="default" size="100%">Bioethics</style></taxonomy><taxonomy><style  face="normal" font="default" size="100%">Privacy and Surveillance </style></taxonomy><taxonomy><style  face="normal" font="default" size="100%">Genetics</style></taxonomy></taxonomies><pubtype><style  face="normal" font="default" size="100%">Audiovisual</style></pubtype><audience-level><style  face="normal" font="default" size="100%">grad</style></audience-level><dates><year><style  face="normal" font="default" size="100%">2002</style></year></dates><isbn><style face="normal" font="default" size="100%">978-0-7365-5381-0</style></isbn><abstract><style face="normal" font="default" size="100%">When it comes to genetic testing, how much should a patient be told? If the news is bad, who else should the patient inform? And should such privileged information be made available to employers, insurance companies, and others? This Fred Friendly Seminar moderated by Harvard Law School's Arthur Miller offers a compelling discource on the far-reaching ethical, social, legal, and economic implications of genetic testing.</style></abstract></record></records></xml>