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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.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/s12098-016-2182-3tr_TR
dc.identifier.issn0019-5456
dc.identifier.urihttp://dx.doi.org/10.1007/s12098-016-2182-3
dc.identifier.urihttp://hdl.handle.net/20.500.11782/114
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...tr_TR
dc.language.isoengtr_TR
dc.publisherSpringer Indiatr_TR
dc.rightsinfo:eu-repo/semantics/closedAccesstr_TR
dc.subjectWilliams-Beuren Syndrometr_TR
dc.subjectDisordertr_TR
dc.titleWilliams-Beuren Syndrome with Mirror Movementstr_TR
dc.typearticletr_TR
dc.relation.journalIndian Journal of Pediatricstr_TR
dc.contributor.departmentHasan Kalyoncu Üniversitesi, Sağlık Bilimleri Yüksek Okulu, Fizyoterapi ve Rehabilitasyon Bölümütr_TR
dc.contributor.authorIDTR150820tr_TR
dc.identifier.issue15 June 2016tr_TR
dc.identifier.startpage1tr_TR
dc.identifier.endpage2tr_TR


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