Please use this identifier to cite or link to this item:
https://hdl.handle.net/11499/5144
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Düzcan, F. | - |
dc.contributor.author | Ergin, H. | - |
dc.contributor.author | Perçin, E.F. | - |
dc.contributor.author | Tepeli, E. | - |
dc.contributor.author | Erkula, G. | - |
dc.date.accessioned | 2019-08-16T11:42:01Z | - |
dc.date.available | 2019-08-16T11:42:01Z | - |
dc.date.issued | 2004 | - |
dc.identifier.issn | 0962-8827 | - |
dc.identifier.uri | https://hdl.handle.net/11499/5144 | - |
dc.identifier.uri | https://doi.org/10.1097/00019605-200401000-00012 | - |
dc.description.abstract | We 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.iso | en | en_US |
dc.relation.ispartof | Clinical Dysmorphology | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Facial asymmetry | en_US |
dc.subject | Femoral deficiency | en_US |
dc.subject | Hypoglossia | en_US |
dc.subject | Micrognathia | en_US |
dc.subject | Preauricular tags | en_US |
dc.subject | agenesis | en_US |
dc.subject | anamnesis | en_US |
dc.subject | article | en_US |
dc.subject | case report | en_US |
dc.subject | clinical feature | en_US |
dc.subject | face malformation | en_US |
dc.subject | femorofacial syndrome | en_US |
dc.subject | femur | en_US |
dc.subject | femur malformation | en_US |
dc.subject | fibula | en_US |
dc.subject | hemifacial microsomia | en_US |
dc.subject | human | en_US |
dc.subject | hypoglossia | en_US |
dc.subject | hypoplasia | en_US |
dc.subject | laboratory test | en_US |
dc.subject | leg | en_US |
dc.subject | male | en_US |
dc.subject | micrognathia | en_US |
dc.subject | philtrum | en_US |
dc.subject | physical examination | en_US |
dc.subject | priority journal | en_US |
dc.subject | radiodiagnosis | en_US |
dc.subject | tongue disease | en_US |
dc.subject | congenital malformation | en_US |
dc.subject | face | en_US |
dc.subject | face asymmetry | en_US |
dc.subject | letter | en_US |
dc.subject | multiple malformation syndrome | en_US |
dc.subject | newborn | en_US |
dc.subject | phocomelia | en_US |
dc.subject | syndrome | en_US |
dc.subject | Abnormalities, Multiple | en_US |
dc.subject | Ectromelia | en_US |
dc.subject | Face | en_US |
dc.subject | Facial Asymmetry | en_US |
dc.subject | Femur | en_US |
dc.subject | Humans | en_US |
dc.subject | Infant, Newborn | en_US |
dc.subject | Male | en_US |
dc.subject | Syndrome | en_US |
dc.title | Femoral-facial syndrome with hemifacial microsomia and hypoglossia | en_US |
dc.type | Article | en_US |
dc.identifier.volume | 13 | en_US |
dc.identifier.issue | 1 | en_US |
dc.identifier.startpage | 43 | |
dc.identifier.startpage | 43 | en_US |
dc.identifier.endpage | 44 | en_US |
dc.identifier.doi | 10.1097/00019605-200401000-00012 | - |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.identifier.pmid | 15127766 | en_US |
dc.identifier.scopus | 2-s2.0-4344718554 | en_US |
dc.identifier.wos | WOS:000220667500012 | en_US |
dc.identifier.scopusquality | Q2 | - |
dc.owner | Pamukkale_University | - |
item.languageiso639-1 | en | - |
item.fulltext | No Fulltext | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.cerifentitytype | Publications | - |
item.openairetype | Article | - |
item.grantfulltext | none | - |
crisitem.author.dept | 14.02. 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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