Investigation of FBN1 gene mutations in clinically diagnosed Marfan's syndrome patients

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dc.contributor.authorCeylan, E.
dc.contributor.authorIsik, E.
dc.contributor.authorSolmaz, A. Ece
dc.contributor.authorAtik, T.
dc.contributor.authorÖzkınay, Ferda
dc.contributor.authorCogulu, O.
dc.contributor.authorOnay, H.
dc.date.accessioned2020-12-01T12:09:15Z
dc.date.available2020-12-01T12:09:15Z
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.description.abstract[No abstract available]en_US
dc.description.sponsorshipEuropean Soc Human Geneten_US
dc.identifier.endpage1880en_US
dc.identifier.issn1018-4813
dc.identifier.issn1476-5438
dc.identifier.startpage1880en_US
dc.identifier.urihttps://hdl.handle.net/11454/63379
dc.identifier.volume27en_US
dc.identifier.wosWOS:000489313907139en_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.titleInvestigation of FBN1 gene mutations in clinically diagnosed Marfan's syndrome patientsen_US
dc.typeConference Objecten_US

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