A CASE WITH 18q DELETION SYNDROME IDENTIFIED WITH B CELL ABSENCE AND CONGENITAL HEART DISEASE

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dc.contributor.authorGuvenc, O.
dc.contributor.authorCimen, D.
dc.contributor.authorKaplan, M. B.
dc.contributor.authorAslan, E.
dc.contributor.authorArtac, H.
dc.contributor.authorAnnagur, A.
dc.date.accessioned2020-03-26T19:00:18Z
dc.date.available2020-03-26T19:00:18Z
dc.date.issued2015
dc.departmentSelçuk Üniversitesien_US
dc.description.abstract[Abstract not Available]en_US
dc.identifier.endpage455en_US
dc.identifier.issn1015-8146en_US
dc.identifier.issue4en_US
dc.identifier.pmid26852518en_US
dc.identifier.scopusqualityN/Aen_US
dc.identifier.startpage451en_US
dc.identifier.urihttps://hdl.handle.net/20.500.12395/31742
dc.identifier.volume26en_US
dc.identifier.wosWOS:000370465300012en_US
dc.identifier.wosqualityQ4en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.publisherMEDECINE ET HYGIENEen_US
dc.relation.ispartofGENETIC COUNSELINGen_US
dc.relation.publicationcategoryDiğeren_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.selcuk20240510_oaigen_US
dc.titleA CASE WITH 18q DELETION SYNDROME IDENTIFIED WITH B CELL ABSENCE AND CONGENITAL HEART DISEASEen_US
dc.typeLetteren_US

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