Congenital hypothyroidism in Rieger Syndrome

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dc.contributor.authorOrnek, Nurgul
dc.contributor.authorOgurel, Reyhan
dc.contributor.authorOrnek, Kemal
dc.date.accessioned2020-06-25T18:16:54Z
dc.date.available2020-06-25T18:16:54Z
dc.date.issued2016
dc.departmentKırıkkale Üniversitesi
dc.descriptionOrnek, Nurgul/0000-0003-3068-1831
dc.description.abstractRieger syndrome (RS) is a multiple malformation syndrome characterized by ocular manifestations and extraocular defects. Herein, we report a 9-year-old boy who exhibited Rieger Syndrome phenotype as well as congenital hypothyroidism which may be an underappreciated feature of RS.en_US
dc.identifier.citationclosedAccessen_US
dc.identifier.doi10.3109/13816810.2014.902079
dc.identifier.endpage88en_US
dc.identifier.issn1381-6810
dc.identifier.issn1744-5094
dc.identifier.issue1en_US
dc.identifier.pmid24666291
dc.identifier.scopus2-s2.0-84960418798
dc.identifier.scopusqualityQ2
dc.identifier.startpage86en_US
dc.identifier.urihttps://doi.org/10.3109/13816810.2014.902079
dc.identifier.urihttps://hdl.handle.net/20.500.12587/6647
dc.identifier.volume37en_US
dc.identifier.wosWOS:000371921400014
dc.identifier.wosqualityQ4
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherTaylor & Francis Incen_US
dc.relation.ispartofOphthalmic Genetics
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectCongenitalen_US
dc.subjecthypothyroidismen_US
dc.subjectRieger Syndromeen_US
dc.titleCongenital hypothyroidism in Rieger Syndromeen_US
dc.typeArticle

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