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dc.creatorSharma, Geetaen
dc.creatorMcCullough, Laurence B.en
dc.creatorChervenak, Frank A.en
dc.date.accessioned2011-07-12T18:20:28Zen
dc.date.available2011-07-12T18:20:28Zen
dc.date.created2007-02-15en
dc.date.issued2007-02-15en
dc.identifier1552-4868en
dc.identifier10.1002/ajmg.c.30118en
dc.identifier.bibliographicCitationAmerican Journal of Medical Genetics. Part C, Seminars in Medical Genetics 2007 February 15; 145C(1): 99-104en
dc.identifier.urihttp://hdl.handle.net/10822/510666en
dc.description.urihttp://dx.doi.org/10.1002/ajmg.c.30118en
dc.formatArticleen
dc.languageengen
dc.source304830en
dc.subjectDisclosureen
dc.subjectRisken
dc.subjectRisk Assessmenten
dc.subjectTrisomyen
dc.subjectTrisomy 21en
dc.subject.classificationTruth-tellingen
dc.subject.classificationGenetic Counseling / Prenatal Diagnosisen
dc.subject.classificationHealth Care for Mentally Disabled Personsen
dc.subject.classificationHealth Care Programs for Womenen
dc.titleEthical considerations of early (first vs. second trimester) risk assessment disclosure for trisomy 21 and patient choice in screening versus diagnostic testing.en
dc.provenanceDigital citation created by the Bioethics Research Library, Georgetown University, for the National Information Resource on Ethics and Human Genetics, a project funded by the United States National Human Genome Research Instituteen
dc.provenanceDigital citation migrated from OpenText Livelink Discovery Server database named GenETHX to DSpace collection GenETHX hosted by Georgetown Universityen


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