The development of a fast newborn screening method for common neonatal metabolic disorders based on nanopore sequencing technology

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dc.contributor.authorOnay, H.
dc.contributor.authorAkgun, B.
dc.contributor.authorYalcinkaya, T.
dc.contributor.authorDilsizoglu, E.
dc.contributor.authorKaya, A. B.
dc.contributor.authorTasar, O.
dc.contributor.authorAtik, T.
dc.date.accessioned2020-12-01T12:09:14Z
dc.date.available2020-12-01T12:09:14Z
dc.date.issued2019
dc.departmentEge Üniversitesien_US
dc.description52nd Conference of the European-Society-of-Human-Genetics (ESHG) -- JUN 15-18, 2019 -- Gothenburg, SWEDENen_US
dc.descriptionAkgun, Bilcag/0000-0002-5220-5652en_US
dc.description.abstract[No abstract available]en_US
dc.description.sponsorshipEuropean Soc Human Geneten_US
dc.identifier.endpage1652en_US
dc.identifier.issn1018-4813
dc.identifier.issn1476-5438
dc.identifier.startpage1651en_US
dc.identifier.urihttps://hdl.handle.net/11454/63375
dc.identifier.volume27en_US
dc.identifier.wosWOS:000489313905083en_US
dc.identifier.wosqualityQ2en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.language.isoenen_US
dc.publisherNature Publishing Groupen_US
dc.relation.ispartofEuropean Journal of Human Geneticsen_US
dc.relation.publicationcategoryKonferans Öğesi - Uluslararası - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.titleThe development of a fast newborn screening method for common neonatal metabolic disorders based on nanopore sequencing technologyen_US
dc.typeConference Objecten_US

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