A unique COL2A1 phenotype as a result of partial gene deletion

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dc.authorid0000-0003-0872-3898
dc.authorid0009-0000-3734-3670
dc.contributor.authorCetin, Sena
dc.contributor.authorGunes, Mustafa
dc.contributor.authorÖzen, Filiz
dc.contributor.authorGulec, Elif Yilmaz
dc.date.accessioned2025-05-10T19:27:36Z
dc.date.issued2023
dc.departmentİstanbul Medeniyet Üniversitesi
dc.description55th European-Society-of-Human-Genetics (ESHG) Conference -- JUN 11-14, 2022 -- Vienna, AUSTRIA
dc.description.abstract[No abstract available]
dc.description.sponsorshipEuropean Soc Human Genet
dc.identifier.endpage399
dc.identifier.issn1018-4813
dc.identifier.issn1476-5438
dc.identifier.scopusqualityQ1
dc.identifier.startpage399
dc.identifier.urihttps://hdl.handle.net/20.500.14730/6973
dc.identifier.volume31
dc.identifier.wosWOS:001050507001318
dc.identifier.wosqualityQ2
dc.indekslendigikaynakWeb of Science
dc.language.isoen
dc.publisherSpringernature
dc.relation.ispartofEuropean Journal of Human Genetics
dc.relation.publicationcategoryKonferans Öğesi - Uluslararası - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WOS_20250302
dc.titleA unique COL2A1 phenotype as a result of partial gene deletion
dc.typeConference Object

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