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dc.contributor.authorDuzcan, F
dc.contributor.authorErgin, H
dc.contributor.authorPercin, EF
dc.contributor.authorTepeli, E
dc.contributor.authorErkula, G
dc.date.accessioned2019-07-27T12:10:23Z
dc.date.accessioned2019-07-28T10:23:00Z
dc.date.available2019-07-27T12:10:23Z
dc.date.available2019-07-28T10:23:00Z
dc.date.issued2004
dc.identifier.issn0962-8827
dc.identifier.urihttps://dx.doi.org/10.1097/01.mcd.0000110534.02258.20
dc.identifier.urihttps://hdl.handle.net/20.500.12418/11270
dc.descriptionWOS: 000220667500012en_US
dc.descriptionPubMed ID: 15127766en_US
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.en_US
dc.language.isoengen_US
dc.publisherLIPPINCOTT WILLIAMS & WILKINSen_US
dc.relation.isversionof10.1097/01.mcd.0000110534.02258.20en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectfemoral deficiencyen_US
dc.subjectfacial asymmetryen_US
dc.subjectmicrognathiaen_US
dc.subjectpreauricular tagsen_US
dc.subjecthypoglossiaen_US
dc.titleFemoral-facial syndrome with hemifacial microsomia and hypoglossiaen_US
dc.typearticleen_US
dc.relation.journalCLINICAL DYSMORPHOLOGYen_US
dc.contributor.departmentPamukkale Univ, Fac Med, Dept Med Biol, Denizli, Turkey -- Pamukkale Univ, Fac Med, Dept Pediat, Denizli, Turkey -- Pamukkale Univ, Fac Med, Dept Orthoped, Denizli, Turkey -- Cumhuriyet Univ, Fac Med, Dept Med Biol & Genet, Sivas, Turkeyen_US
dc.contributor.authorIDPercin, Ferda -- 0000-0001-9317-8155en_US
dc.identifier.volume13en_US
dc.identifier.issue1en_US
dc.identifier.endpage44en_US
dc.identifier.startpage43en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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