Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/25154
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dc.date.accessioned2022-03-17T13:46:27Z-
dc.date.available2022-03-17T13:46:27Z-
dc.date.issued2005-
dc.identifier.citationÖzbek, S. vd. (2005). "Marden-Walker syndrome with some additional anomalies". Pediatrics International, 47(1), 92-94.en_US
dc.identifier.issn1328-8067-
dc.identifier.issn1442-200X-
dc.identifier.urihttps://doi.org/10.1111/j.1442-200x.2004.02010.x-
dc.identifier.urihttps://onlinelibrary.wiley.com/doi/10.1111/j.1442-200x.2004.02010.x-
dc.identifier.urihttp://hdl.handle.net/11452/25154-
dc.language.isoenen_US
dc.publisherWileyen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectPediatricsen_US
dc.subjectCleft palateen_US
dc.subjectExpressionless faceen_US
dc.subjectMarden-walker syndromeen_US
dc.subjectPlenoidal sinusen_US
dc.subjectShort frenulumen_US
dc.subjectSpectrumen_US
dc.subjectAbnormalitiesen_US
dc.subjectPhenotypeen_US
dc.subject.meshAbnormalities, multipleen_US
dc.subject.meshCleft palateen_US
dc.subject.meshDiseases in twinsen_US
dc.subject.meshFacial expressionen_US
dc.subject.meshFemaleen_US
dc.subject.meshHumansen_US
dc.subject.meshInfanten_US
dc.subject.meshSyndromeen_US
dc.subject.meshTurkeyen_US
dc.titleMarden-Walker syndrome with some additional anomaliesen_US
dc.typeArticleen_US
dc.identifier.wos000226654400019tr_TR
dc.identifier.scopus2-s2.0-14644429704tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Plastik Cerrahi Anabilim Dalı.tr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Çocuk Endokrinoloji Anabilim Dalı.tr_TR
dc.contributor.orcid0000-0003-0710-5422tr_TR
dc.identifier.startpage92tr_TR
dc.identifier.endpage94tr_TR
dc.identifier.volume47tr_TR
dc.identifier.issue1tr_TR
dc.relation.journalPediatrics Internationalen_US
dc.contributor.buuauthorÖzbek, Serhat-
dc.contributor.buuauthorSağlam, Halil-
dc.contributor.buuauthorÖzdamar, Erkut-
dc.contributor.researcheridC-7392-2019tr_TR
dc.contributor.researcheridAAH-5441-2021tr_TR
dc.identifier.pubmed15693875tr_TR
dc.subject.wosPediatricsen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.indexed.pubmedPubmeden_US
dc.wos.quartileQ4en_US
dc.contributor.scopusid7005245657tr_TR
dc.contributor.scopusid35612700100tr_TR
dc.contributor.scopusid6508120107tr_TR
dc.subject.scopusArthrogryposis; Freeman-Sheldon Syndrome; Fetal Movementen_US
dc.subject.emtreeArticleen_US
dc.subject.emtreeBirth weighten_US
dc.subject.emtreeCase reporten_US
dc.subject.emtreeChromosome analysisen_US
dc.subject.emtreeCleft palateen_US
dc.subject.emtreeClinical featureen_US
dc.subject.emtreeCongenital malformationen_US
dc.subject.emtreeEchocardiographyen_US
dc.subject.emtreeFace malformationen_US
dc.subject.emtreeFemaleen_US
dc.subject.emtreeGestational ageen_US
dc.subject.emtreeHallux valgusen_US
dc.subject.emtreeHeart atrium septum defecten_US
dc.subject.emtreeHumanen_US
dc.subject.emtreeInfanten_US
dc.subject.emtreeMarden walker syndromeen_US
dc.subject.emtreeNuclear magnetic resonance imagingen_US
dc.subject.emtreePes equinovarusen_US
dc.subject.emtreePhysical examinationen_US
dc.subject.emtreePregnancyen_US
dc.subject.emtreePriority journalen_US
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