Demonstration of uniparental-isodisomy on chromosome 22q11.2 in a patient with childhood schizophrenia and facial dysmorphology by whole-genome analysis

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dc.contributor.authorCogulu O.
dc.contributor.authorPariltay E.
dc.contributor.authorDurmaz A.A.
dc.contributor.authorAykut A.
dc.contributor.authorGunduz C.
dc.contributor.authorOzbaran B.
dc.contributor.authorAydin H.H.
dc.contributor.authorErermis S.
dc.contributor.authorAydin C.
dc.contributor.authorÖzkınay F.
dc.date.accessioned2019-10-27T08:33:08Z
dc.date.available2019-10-27T08:33:08Z
dc.date.issued2012
dc.departmentEge Üniversitesien_US
dc.description.abstract[No abstract available]en_US
dc.identifier.doi10.1176/appi.neuropsych.11010027en_US
dc.identifier.endpageE14en_US
dc.identifier.issn0895-0172
dc.identifier.issue1en_US
dc.identifier.pmid22450627en_US
dc.identifier.scopusqualityQ2en_US
dc.identifier.startpageE13en_US
dc.identifier.urihttps://doi.org/10.1176/appi.neuropsych.11010027
dc.identifier.urihttps://hdl.handle.net/11454/26666
dc.identifier.volume24en_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.relation.ispartofJournal of Neuropsychiatry and Clinical Neurosciencesen_US
dc.relation.publicationcategoryDiğeren_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.titleDemonstration of uniparental-isodisomy on chromosome 22q11.2 in a patient with childhood schizophrenia and facial dysmorphology by whole-genome analysisen_US
dc.typeLetteren_US

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