Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/5003
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dc.contributor.authorKılıç, İlknur.-
dc.contributor.authorBaykara, Y.-
dc.contributor.authorSemerci, Cavidan Nur.-
dc.contributor.authorErgin, Hacer.-
dc.contributor.authorTufan Şatıroğlu, N. Lale-
dc.date.accessioned2019-08-16T11:39:53Z-
dc.date.available2019-08-16T11:39:53Z-
dc.date.issued2004-
dc.identifier.issn1300-0144-
dc.identifier.urihttps://hdl.handle.net/11499/5003-
dc.description.abstractAbstract Not Availableen_US
dc.language.isoenen_US
dc.relation.ispartofTurkish Journal of Medical Sciencesen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectApert syndromeen_US
dc.subjectFGFR2 mutationen_US
dc.subjectfibroblast growth factor receptor 2en_US
dc.subjectacrocephalosyndactylyen_US
dc.subjectarticleen_US
dc.subjectcase reporten_US
dc.subjectcraniofacial synostosisen_US
dc.subjectface malformationen_US
dc.subjectgene mutationen_US
dc.subjectgenetic analysisen_US
dc.subjectheart atrium septum defecten_US
dc.subjecthumanen_US
dc.subjectmaleen_US
dc.subjectnewbornen_US
dc.subjectsyndactylyen_US
dc.subjectTurkey (republic)en_US
dc.titleApert syndromeen_US
dc.typeArticleen_US
dc.identifier.volume34en_US
dc.identifier.issue6en_US
dc.identifier.startpage405en_US
dc.identifier.endpage408en_US
dc.authorid36835035474-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.trdizinid52925en_US
dc.identifier.scopusqualityQ3-
dc.ownerPamukkale_University-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypeArticle-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.languageiso639-1en-
crisitem.author.dept14.02. Internal Medicine-
crisitem.author.dept14.02. Internal Medicine-
Appears in Collections:Tıp Fakültesi Koleksiyonu
TR Dizin İndeksli Yayınlar Koleksiyonu / TR Dizin Indexed Publications Collection
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