Browsing Sivas Cumhuriyet Üniversitesi Edebiyat Fakültesi by Subject "Whole-exome sequencing"
Now showing items 1-1 of 1
-
Mutation in MEOX1 gene causes a recessive Klippel-Feil syndrome subtype
(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 ...