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Survey of Informed Consent for Registration of Congenital Anomalies in Europe

dc.creatorBusby, Aracelien
dc.creatorRitvanen, Annukkaen
dc.creatorDolk, Helenen
dc.creatorArmstrong, Nicolaen
dc.creatorDe Walle, Hermienen
dc.creatorRiano-Galan, Isolinaen
dc.creatorGatt, Miriamen
dc.creatorMcDonnell, Roberten
dc.creatorNelen, Veraen
dc.creatorStone, Daviden
dc.date.accessioned2016-01-08T23:41:25Zen
dc.date.available2016-01-08T23:41:25Zen
dc.date.created2005-07-16en
dc.date.issued2005-07-16en
dc.identifierdoi:10.1136/bmj.331.7509.140en
dc.identifier.bibliographicCitationBMJ: British Medical Journal 2005 July 16; 331(7509): 140-141en
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=Survey+of+informed+consent+for+registration+of+congenital+anomalies+in+Europe&title=BMJ:+British+Medical+Journal+&volume=331&issue=7509&date=2005-07&au=Busby,+Araceli;+Ritvanen,+Annukka;+Dolk,+Helen;+Armstrong,+Nicola;+De+Walle,+Hermien;+Riano-Galan,+Isolina;+Gatt,+Miriam;+McDonnell,+Robert;+Nelen,+Vera;+Stone,+Daviden
dc.identifier.urihttp://dx.doi.org/10.1136/bmj.331.7509.140en
dc.identifier.urihttp://hdl.handle.net/10822/980211en
dc.formatArticleen
dc.languageenen
dc.sourceeweb:286592en
dc.subjectConsenten
dc.subjectInformed Consenten
dc.subjectSurveyen
dc.subject.classificationConfidentialityen
dc.subject.classificationInternational and Political Dimensions of Biology and Medicineen
dc.subject.classificationInformation Science Ethicsen
dc.subject.classificationMinors / Parental Consenten
dc.titleSurvey of Informed Consent for Registration of Congenital Anomalies in Europeen
dc.provenanceCitation prepared by the Library and Information Services group of the Kennedy Institute of Ethics, Georgetown University for the ETHXWeb database.en
dc.provenanceCitation migrated from OpenText LiveLink Discovery Server database named EWEB hosted by the Bioethics Research Library to the DSpace collection EthxWeb hosted by DigitalGeorgetown.en


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