Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/5144
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dc.contributor.authorDüzcan, F.-
dc.contributor.authorErgin, H.-
dc.contributor.authorPerçin, E.F.-
dc.contributor.authorTepeli, E.-
dc.contributor.authorErkula, G.-
dc.date.accessioned2019-08-16T11:42:01Z-
dc.date.available2019-08-16T11:42:01Z-
dc.date.issued2004-
dc.identifier.issn0962-8827-
dc.identifier.urihttps://hdl.handle.net/11499/5144-
dc.identifier.urihttps://doi.org/10.1097/00019605-200401000-00012-
dc.description.abstractWe present a boy diagnosed as femoral-facial syndrome with total agenesis of right lower limb, agenesis of femur and fibula of left lower limb and micrognathia, long philtrum as facial features. Some additional features were described as hemifacial microsomia, preauricular tags and hypoglossia. © 2004 Lippincott Williams & Wilkins.en_US
dc.language.isoenen_US
dc.relation.ispartofClinical Dysmorphologyen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectFacial asymmetryen_US
dc.subjectFemoral deficiencyen_US
dc.subjectHypoglossiaen_US
dc.subjectMicrognathiaen_US
dc.subjectPreauricular tagsen_US
dc.subjectagenesisen_US
dc.subjectanamnesisen_US
dc.subjectarticleen_US
dc.subjectcase reporten_US
dc.subjectclinical featureen_US
dc.subjectface malformationen_US
dc.subjectfemorofacial syndromeen_US
dc.subjectfemuren_US
dc.subjectfemur malformationen_US
dc.subjectfibulaen_US
dc.subjecthemifacial microsomiaen_US
dc.subjecthumanen_US
dc.subjecthypoglossiaen_US
dc.subjecthypoplasiaen_US
dc.subjectlaboratory testen_US
dc.subjectlegen_US
dc.subjectmaleen_US
dc.subjectmicrognathiaen_US
dc.subjectphiltrumen_US
dc.subjectphysical examinationen_US
dc.subjectpriority journalen_US
dc.subjectradiodiagnosisen_US
dc.subjecttongue diseaseen_US
dc.subjectcongenital malformationen_US
dc.subjectfaceen_US
dc.subjectface asymmetryen_US
dc.subjectletteren_US
dc.subjectmultiple malformation syndromeen_US
dc.subjectnewbornen_US
dc.subjectphocomeliaen_US
dc.subjectsyndromeen_US
dc.subjectAbnormalities, Multipleen_US
dc.subjectEctromeliaen_US
dc.subjectFaceen_US
dc.subjectFacial Asymmetryen_US
dc.subjectFemuren_US
dc.subjectHumansen_US
dc.subjectInfant, Newbornen_US
dc.subjectMaleen_US
dc.subjectSyndromeen_US
dc.titleFemoral-facial syndrome with hemifacial microsomia and hypoglossiaen_US
dc.typeArticleen_US
dc.identifier.volume13en_US
dc.identifier.issue1en_US
dc.identifier.startpage43
dc.identifier.startpage43en_US
dc.identifier.endpage44en_US
dc.identifier.doi10.1097/00019605-200401000-00012-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.pmid15127766en_US
dc.identifier.scopus2-s2.0-4344718554en_US
dc.identifier.wosWOS:000220667500012en_US
dc.identifier.scopusqualityQ2-
dc.ownerPamukkale_University-
item.languageiso639-1en-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypeArticle-
crisitem.author.dept14.02. Internal Medicine-
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
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