Williams-Beuren Syndrome with Mirror Movements

dc.contributor.authorIşıkay, Sedat
dc.contributor.authorSezer, Sadettin
dc.contributor.authorKırık, Serkan
dc.contributor.authorGüngör, Olcay
dc.date.accessioned2016-08-16T08:37:42Z
dc.date.available2016-08-16T08:37:42Z
dc.date.issued2016-06
dc.departmentHKÜ, Sağlık Bilimleri Yüksekokulu, Fizyoterapi ve Rehabilitasyon Bölümüen_US
dc.description.abstractTo the Editor: Williams-Beuren Syndrome (WBS) is a rare neurodevelopmental disorder caused by deletion of chromosome 7 at q11.23. It is characterized by distinctive facies, congenital cardiovascular malformations, intellectual disabilities, and various other manifestations [1, 2]. Here, we present a child with WBS who presented with abnormal involuntary hand movements...en_US
dc.identifier.citationIşıkay, S., Sezer, S., Kırık, S., & Güngör, O. (2016). Williams-beuren syndrome with mirror movements. Indian Journal of Pediatrics, , 1-2. doi:10.1007/s12098-016-2182-3en_US
dc.identifier.endpage2en_US
dc.identifier.issn0019-5456
dc.identifier.issue15 June 2016en_US
dc.identifier.orcidTR150820en_US
dc.identifier.pmid27306224
dc.identifier.scopus2-s2.0-84974855949
dc.identifier.scopusqualityQ2
dc.identifier.startpage1en_US
dc.identifier.urihttp://dx.doi.org/10.1007/s12098-016-2182-3
dc.identifier.urihttps://hdl.handle.net/20.500.11782/114
dc.identifier.wosWOS:000392939500026
dc.identifier.wosqualityQ4
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherSpringer Indiaen_US
dc.relation.ispartofIndian Journal of Pediatrics
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectWilliams-Beuren Syndromeen_US
dc.subjectDisorderen_US
dc.titleWilliams-Beuren Syndrome with Mirror Movements
dc.typeArticle

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