1. Açık Erişim@BUU
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Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/31727
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dc.date.accessioned2023-03-24T07:48:22Z-
dc.date.available2023-03-24T07:48:22Z-
dc.date.issued2003-12-
dc.identifier.citationNacarküçük, E. vd. (2003). “Opitz trigonocephaly C syndrome associated with hearing loss”. Pediatrics International, 45(6), 731-733.en_US
dc.identifier.issn1328-8067-
dc.identifier.urihttps://doi.org/10.1111/j.1442-200X.2003.01819.x-
dc.identifier.urihttps://onlinelibrary.wiley.com/doi/10.1111/j.1442-200X.2003.01819.x-
dc.identifier.urihttp://hdl.handle.net/11452/31727-
dc.language.isoenen_US
dc.publisherWileyen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectPediatricsen_US
dc.subjectC syndromeen_US
dc.subjectHearing lossen_US
dc.subject.meshAbnormalities, multipleen_US
dc.subject.meshCraniosynostosesen_US
dc.subject.meshFemaleen_US
dc.subject.meshHearing lossen_US
dc.subject.meshHumansen_US
dc.subject.meshInfanten_US
dc.subject.meshMental retardationen_US
dc.subject.meshSyndromeen_US
dc.titleOpitz trigonocephaly C syndrome associated with hearing lossen_US
dc.typeArticleen_US
dc.identifier.wos000187156100018tr_TR
dc.identifier.scopus2-s2.0-1642521752tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Çocuk Sağlığı ve Hastalıkları Anabilim Dalı.tr_TR
dc.identifier.startpage731tr_TR
dc.identifier.endpage733tr_TR
dc.identifier.volume45tr_TR
dc.identifier.issue6tr_TR
dc.relation.journalPedi̇atri̇cs Internati̇onalen_US
dc.contributor.buuauthorNacarküçük, Ergün-
dc.contributor.buuauthorOkan, Mehmet-
dc.contributor.buuauthorSarimehmet, Handan-
dc.contributor.buuauthorOzer, Tülay-
dc.identifier.pubmed14651551tr_TR
dc.subject.wosPediatricsen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.indexed.pubmedPubMeden_US
dc.wos.quartileQ4en_US
dc.contributor.scopusid6602924559tr_TR
dc.contributor.scopusid6701707256tr_TR
dc.contributor.scopusid6507052972tr_TR
dc.contributor.scopusid36730320700tr_TR
dc.subject.emtreeAdolescenten_US
dc.subject.emtreeAgenesisen_US
dc.subject.emtreeAnamnesisen_US
dc.subject.emtreeArticleen_US
dc.subject.emtreeBrain atrophyen_US
dc.subject.emtreeCase reporten_US
dc.subject.emtreeChromosome analysisen_US
dc.subject.emtreeClinical featureen_US
dc.subject.emtreeCongenital malformationen_US
dc.subject.emtreeCorpus callosumen_US
dc.subject.emtreeDevelopmental disorderen_US
dc.subject.emtreeElectroencephalogramen_US
dc.subject.emtreeEpileptic stateen_US
dc.subject.emtreeFace malformationen_US
dc.subject.emtreeFaciesen_US
dc.subject.emtreeFemaleen_US
dc.subject.emtreeHearing lossen_US
dc.subject.emtreeHumanen_US
dc.subject.emtreeLaboratory testen_US
dc.subject.emtreeMental deficiencyen_US
dc.subject.emtreeOpitz syndromeen_US
dc.subject.emtreeOpitz trigonocephaly c syndromeen_US
dc.subject.emtreePatient referralen_US
dc.subject.emtreePhysical examinationen_US
dc.subject.emtreePriority journalen_US
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