First Turkish Patient with Feingold Syndrome Type 2 with severe motor mental retardation, epilepsy

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dc.contributor.authorHazan, F.
dc.contributor.authorOzyilmaz, B.
dc.contributor.authorSubasioglu, A.
dc.contributor.authorKirbiyik, O.
dc.contributor.authorAykut, A.
dc.date.accessioned2021-05-03T20:41:34Z
dc.date.available2021-05-03T20:41:34Z
dc.date.issued2018
dc.departmentEge Üniversitesien_US
dc.description50th European-Society-of-Human-Genetics (ESHG) Conference -- MAY 27-30, 2017 -- Copenhagen, DENMARKen_US
dc.descriptionOzyilmaz, Berk/0000-0003-2654-3698; AYKUT, Ayca/0000-0002-1460-0053en_US
dc.description.abstract[No Abstract Available]en_US
dc.description.sponsorshipEuropean Soc Human Geneten_US
dc.identifier.endpage470en_US
dc.identifier.issn1018-4813
dc.identifier.issn1476-5438
dc.identifier.startpage470en_US
dc.identifier.urihttps://hdl.handle.net/11454/70610
dc.identifier.volume26en_US
dc.identifier.wosWOS:000489312604095en_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 Keyword]en_US
dc.titleFirst Turkish Patient with Feingold Syndrome Type 2 with severe motor mental retardation, epilepsyen_US
dc.typeConference Objecten_US

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