Please use this identifier to cite or link to this item: http://dx.doi.org/10.25673/101550
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dc.contributor.authorRosenau, Henning-
dc.contributor.authorSteffen, Felicia-
dc.date.accessioned2023-03-29T06:40:50Z-
dc.date.available2023-03-29T06:40:50Z-
dc.date.issued2022-
dc.identifier.urihttps://opendata.uni-halle.de//handle/1981185920/103508-
dc.identifier.urihttp://dx.doi.org/10.25673/101550-
dc.description.abstractNewborn screening is used for the early detection of diseases in newborns and enables rapid intervention to prevent serious consequences, including infant death. Since the Genetic Diagnostics Act came into force in 2010, the rules of the Act have applied to newborn screening. Over the years since the Act came into force, some legal issues have been resolved, but new legal aspects have also arisen for which the Act does not yet provide a solution.eng
dc.language.isoeng-
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/-
dc.subject.ddc176-
dc.titleLegal aspects of newborn screeningeng
dc.typeArticle-
local.versionTypepublishedVersion-
local.bibliographicCitation.journaltitleMedizinische Genetik-
local.bibliographicCitation.volume34-
local.bibliographicCitation.issue1-
local.bibliographicCitation.pagestart3-
local.bibliographicCitation.pageend11-
local.bibliographicCitation.publishernamede Gruyter-
local.bibliographicCitation.publisherplaceBerlin-
local.bibliographicCitation.doi10.1515/medgen-2022-2110-
local.subject.keywordsnewborn screening, Genetic Diagnostics Act, informed consent, incidental findings-
local.openaccesstrue-
dc.identifier.ppn1804092916-
local.bibliographicCitation.year2022-
cbs.sru.importDate2023-03-29T06:39:00Z-
local.bibliographicCitationEnthalten in Medizinische Genetik - Berlin : de Gruyter, 1998-
local.accessrights.dnbfree-
Appears in Collections:Open Access Publikationen der MLU

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