Different phenotype with 22q13.3 deletion syndrome in two patients

Basit Öğe Kaydı
dc.authoridatli, emine ikbal/0000-0001-9003-1449
dc.authoridGürkan, Hakan/0000-0002-8967-6124
dc.authorwosidDemir, Selma/A-1500-2018
dc.authorwosidatli, emine ikbal/AAN-5060-2020
dc.authorwosideker, damla/AAE-6947-2020
dc.authorwosidGürkan, Hakan/AAF-2866-2020
dc.contributor.authorGurkan, H.
dc.contributor.authorAtli, E.
dc.contributor.authorAtli, E.
dc.contributor.authorDemir, S.
dc.contributor.authorOzen, Y.
dc.contributor.authorTozkir, H.
dc.contributor.authorEker, D.
dc.date.accessioned2024-06-12T11:23:00Z
dc.date.available2024-06-12T11:23:00Z
dc.date.issued2019
dc.departmentTrakya Üniversitesien_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 Available]en_US
dc.description.sponsorshipEuropean Soc Human Geneten_US
dc.identifier.endpage942en_US
dc.identifier.issn1018-4813
dc.identifier.issn1476-5438
dc.identifier.startpage941en_US
dc.identifier.urihttps://hdl.handle.net/20.500.14551/26182
dc.identifier.volume27en_US
dc.identifier.wosWOS:000489313107155en_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[No Keywords]en_US
dc.titleDifferent phenotype with 22q13.3 deletion syndrome in two patientsen_US
dc.typeConference Objecten_US

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