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dc.creatorVictoroff, Michael S.en
dc.date.accessioned2015-05-05T18:29:19Zen
dc.date.available2015-05-05T18:29:19Zen
dc.date.created1992-03-26en
dc.date.issued1992-03-26en
dc.identifier.bibliographicCitationNew England Journal of Medicine. 1992 Mar 26; 326(13): 896-897.en
dc.identifier.issn0028-4793en
dc.identifier.urihttp://worldcatlibraries.org/registry/gateway?version=1.0&url_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&atitle=How+to+Inform+Patients+That+They+Cannot+Be+Informed&title=New+England+Journal+of+Medicine.++&volume=326&issue=13&pages=896-897&date=1992&au=Victoroff,+Michael+S.en
dc.identifier.urihttp://hdl.handle.net/10822/735094en
dc.formatArticleen
dc.languageenen
dc.sourceBRL:KIE/35940en
dc.subjectAbortionen
dc.subjectAlternativesen
dc.subjectCounselingen
dc.subjectConsenten
dc.subjectDisclosureen
dc.subjectFederal Governmenten
dc.subjectGovernmenten
dc.subjectGovernment Regulationen
dc.subjectHealthen
dc.subjectHealth Facilitiesen
dc.subjectInformed Consenten
dc.subjectLegal Aspectsen
dc.subjectPatientsen
dc.subjectPhysiciansen
dc.subjectRegulationen
dc.subjectReproductionen
dc.subjectRisks and Benefitsen
dc.titleHow to Inform Patients That They Cannot Be Informeden
dc.provenanceDigital citation created by the National Reference Center for Bioethics Literature at Georgetown University for the BIOETHICSLINE database, part of the Kennedy Institute of Ethics' Bioethics Information Retrieval Project funded by the United States National Library of Medicine.en
dc.provenanceDigital citation migrated from OpenText LiveLink Discovery Server database named NBIO hosted by the Bioethics Research Library to the DSpace collection BioethicsLine hosted by Georgetown University.en


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