The prevalance of 22q11.2 deletion in children with congenital heart disease and dismorphic features

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dc.contributor.authorKaya
dc.contributor.authorCankaya, Tufan
dc.contributor.authorYilmaz, Elif
dc.contributor.authorOztunc, Funda
dc.contributor.authorTuysuz, Beyhan
dc.date.accessioned2019-10-27T19:37:14Z
dc.date.available2019-10-27T19:37:14Z
dc.date.issued2007
dc.departmentEge Üniversitesien_US
dc.description6th European Cytogenetics Conference -- JUL 07-10, 2007 -- Istanbul, TURKEYen_US
dc.identifier.endpage77en_US
dc.identifier.issn0967-3849
dc.identifier.startpage77en_US
dc.identifier.urihttps://hdl.handle.net/11454/39950
dc.identifier.volume15en_US
dc.identifier.wosWOS:000248859800164en_US
dc.identifier.wosqualityQ2en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.language.isoenen_US
dc.publisherSpringeren_US
dc.relation.ispartofChromosome Researchen_US
dc.relation.publicationcategoryKonferans Öğesi - Uluslararası - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.titleThe prevalance of 22q11.2 deletion in children with congenital heart disease and dismorphic featuresen_US
dc.typeConference Objecten_US

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