A rare hereditary connective tissue disease associated with the TGF-? signalling pathway:a case study of Loeys-Dietz syndrome type 1

Basit Öğe Kaydı
dc.contributor.authorBalasar, M.
dc.contributor.authorOflaz, M. B.
dc.contributor.authorEmlik, G. D.
dc.date.accessioned2024-02-23T14:45:15Z
dc.date.available2024-02-23T14:45:15Z
dc.date.issued2019
dc.departmentNEÜen_US
dc.description51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG) -- JUN 16-19, 2018 -- Milan, ITALYen_US
dc.description.abstract[Abstract Not Availabe]en_US
dc.description.sponsorshipEuropean Soc Human Geneten_US
dc.identifier.endpage914en_US
dc.identifier.issn1018-4813
dc.identifier.issn1476-5438
dc.identifier.scopusqualityQ1en_US
dc.identifier.startpage914en_US
dc.identifier.urihttps://hdl.handle.net/20.500.12452/17334
dc.identifier.volume27en_US
dc.identifier.wosWOS:000489313107095en_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.subject[Keyword Not Available]en_US
dc.titleA rare hereditary connective tissue disease associated with the TGF-? signalling pathway:a case study of Loeys-Dietz syndrome type 1en_US
dc.typeConference Objecten_US

Dosyalar

Koleksiyon

WoS İndeksli Yayınlar Koleksiyonu