Yayın: Opitz trigonocephaly C syndrome associated with hearing loss
| dc.contributor.buuauthor | Nacarküçük, Ergün | |
| dc.contributor.buuauthor | Okan, Mehmet | |
| dc.contributor.buuauthor | Sarimehmet, Handan | |
| dc.contributor.buuauthor | Ozer, Tülay | |
| dc.contributor.department | Tıp Fakültesi | |
| dc.contributor.department | Çocuk Sağlığı ve Hastalıkları Ana Bilim Dalı | |
| dc.contributor.scopusid | 6602924559 | |
| dc.contributor.scopusid | 6701707256 | |
| dc.contributor.scopusid | 6507052972 | |
| dc.contributor.scopusid | 36730320700 | |
| dc.date.accessioned | 2023-03-24T07:48:22Z | |
| dc.date.available | 2023-03-24T07:48:22Z | |
| dc.date.issued | 2003-12 | |
| dc.identifier.citation | Nacarküçük, E. vd. (2003). “Opitz trigonocephaly C syndrome associated with hearing loss”. Pediatrics International, 45(6), 731-733. | |
| dc.identifier.doi | 10.1111/j.1442-200X.2003.01819.x | |
| dc.identifier.endpage | 733 | |
| dc.identifier.issn | 1328-8067 | |
| dc.identifier.issue | 6 | |
| dc.identifier.pubmed | 14651551 | |
| dc.identifier.scopus | 2-s2.0-1642521752 | |
| dc.identifier.startpage | 731 | |
| dc.identifier.uri | https://doi.org/10.1111/j.1442-200X.2003.01819.x | |
| dc.identifier.uri | https://onlinelibrary.wiley.com/doi/10.1111/j.1442-200X.2003.01819.x | |
| dc.identifier.uri | http://hdl.handle.net/11452/31727 | |
| dc.identifier.volume | 45 | |
| dc.identifier.wos | 000187156100018 | |
| dc.indexed.wos | SCIE | |
| dc.language.iso | en | |
| dc.publisher | Wiley | |
| dc.relation.journal | Pedi̇atri̇cs Internati̇onal | |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi | |
| dc.rights | info:eu-repo/semantics/closedAccess | |
| dc.subject | Pediatrics | |
| dc.subject | C syndrome | |
| dc.subject | Hearing loss | |
| dc.subject.emtree | Adolescent | |
| dc.subject.emtree | Agenesis | |
| dc.subject.emtree | Anamnesis | |
| dc.subject.emtree | Article | |
| dc.subject.emtree | Brain atrophy | |
| dc.subject.emtree | Case report | |
| dc.subject.emtree | Chromosome analysis | |
| dc.subject.emtree | Clinical feature | |
| dc.subject.emtree | Congenital malformation | |
| dc.subject.emtree | Corpus callosum | |
| dc.subject.emtree | Developmental disorder | |
| dc.subject.emtree | Electroencephalogram | |
| dc.subject.emtree | Epileptic state | |
| dc.subject.emtree | Face malformation | |
| dc.subject.emtree | Facies | |
| dc.subject.emtree | Female | |
| dc.subject.emtree | Hearing loss | |
| dc.subject.emtree | Human | |
| dc.subject.emtree | Laboratory test | |
| dc.subject.emtree | Mental deficiency | |
| dc.subject.emtree | Opitz syndrome | |
| dc.subject.emtree | Opitz trigonocephaly c syndrome | |
| dc.subject.emtree | Patient referral | |
| dc.subject.emtree | Physical examination | |
| dc.subject.emtree | Priority journal | |
| dc.subject.mesh | Abnormalities, multiple | |
| dc.subject.mesh | Craniosynostoses | |
| dc.subject.mesh | Female | |
| dc.subject.mesh | Hearing loss | |
| dc.subject.mesh | Humans | |
| dc.subject.mesh | Infant | |
| dc.subject.mesh | Mental retardation | |
| dc.subject.mesh | Syndrome | |
| dc.subject.wos | Pediatrics | |
| dc.title | Opitz trigonocephaly C syndrome associated with hearing loss | |
| dc.type | Article | |
| dc.wos.quartile | Q4 | |
| dspace.entity.type | Publication | |
| local.contributor.department | Tıp Fakültesi/Çocuk Sağlığı ve Hastalıkları Ana Bilim Dalı | |
| local.indexed.at | Scopus | |
| local.indexed.at | WOS |
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