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, Ozgur
dc.contributor.authorPariltay, Erhan
dc.contributor.authorDurmaz, Asude Alpman
dc.contributor.authorAykut, Ayca
dc.contributor.authorGunduz, Cumhur
dc.contributor.authorOzbaran, Burcu
dc.contributor.authorAydin, Hikmet Hakan
dc.contributor.authorErermis, Serpil
dc.contributor.authorAydin, Cahide
dc.contributor.authorÖzkınay, Ferda
dc.date.accessioned2019-10-27T21:40:48Z
dc.date.available2019-10-27T21:40:48Z
dc.date.issued2012
dc.departmentEge Üniversitesien_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.startpageE13en_US
dc.identifier.urihttps://doi.org/10.1176/appi.neuropsych.11010027
dc.identifier.urihttps://hdl.handle.net/11454/46372
dc.identifier.volume24en_US
dc.identifier.wosWOS:000302731500008en_US
dc.identifier.wosqualityQ2en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.publisherAmer Psychiatric Publishing, Incen_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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