Browsing Tarih Bölümü by Author "Kazanci, Burak"

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Mutation in MEOX1 gene causes a recessive Klippel-Feil syndrome subtype

Bayrakli, Fatih; Guclu, Bulent; Yakicier, Cengiz; Balaban, Hatice; Kartal, Ugur; Erguner, Bekir; Sagiroglu, Mahmut Samil; Yuksel, Sirin; Ozturk, Ahmet Rasit; Kazanci, Burak; Ozum, Unal; Kars, Hamit Zafer (BIOMED CENTRAL LTD, 2013)

Background: Klippel-Feil syndrome (KFS) is characterized by the developmental failure of the cervical spine and has two dominantly inherited subtypes. Affected individuals who are the children of a consanguineous marriage ...