Show simple item record

dc.creatorHelm, David T.en
dc.creatorMiranda, Saraen
dc.creatorChedd, Naomi Angoffen
dc.date.accessioned2011-07-12T18:35:10Zen
dc.date.available2011-07-12T18:35:10Zen
dc.date.created1998-01en
dc.date.issued1998-01en
dc.identifier.bibliographicCitationMental Retardation 1998 February; 36(1): 55-61en
dc.identifier.urihttp://hdl.handle.net/10822/532439en
dc.formatArticleen
dc.languageengen
dc.source186030en
dc.subjectDiagnosisen
dc.subjectDown Syndromeen
dc.subjectMothersen
dc.subjectPrenatal Diagnosisen
dc.subject.classificationGenetic Counseling / Prenatal Diagnosisen
dc.subject.classificationHealth Care for Mentally Disabled Personsen
dc.subject.classificationHealth Care for Embryos and Fetusesen
dc.titlePrenatal Diagnosis of Down Syndrome: Mothers' Reflections on Supports Needed from Diagnosis to Birthen
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


This item appears in the following Collection(s)

Show simple item record


Georgetown University Seal
©2009—2019 Bioethics Research Library
Box 571212 Washington DC 20057-1212
202.687.3885