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dc.contributor.editorStern, Karin S.en
dc.contributor.editorDavis, Jessica G.en
dc.date.accessioned2011-07-12T18:41:59Zen
dc.date.available2011-07-12T18:41:59Zen
dc.date.created1994en
dc.date.issued1994en
dc.identifier.bibliographicCitationNew York: Council of Regional Networks for Genetic Services [CORN], 1994. 223 p.en
dc.identifier.urihttp://hdl.handle.net/10822/545598en
dc.formatMonographen
dc.languageengen
dc.source136522en
dc.subjectDiseaseen
dc.subject.classificationGenetic Counseling / Prenatal Diagnosisen
dc.subject.classificationGenetic Screening / Genetic Testingen
dc.subject.classificationNeurosciences and Mental Health Therapiesen
dc.subject.classificationHealth Care for Newborns and Minorsen
dc.titleNEWBORN SCREENING FOR SICKLE CELL DISEASE: ISSUES AND IMPLICATIONSen
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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