Browsing by Author "Sezer, Sadettin"
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Williams-Beuren Syndrome with Mirror Movements
Işıkay, Sedat; Sezer, Sadettin; Kırık, Serkan; Güngör, Olcay (Springer India, 2016-06)To 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 ...