Yazar "Yılmaz G.C." için listeleme

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A case report of xp21 contiguous gene syndrome: Adrenal hypoplasia congenita, glycerol kinase deficiency, and duchenne muscular dystrophy

Kara C.; Yılmaz G.C.; Bitkin E.Ç.; Aydın M. (Galenos Yayincilik,, 2016)

Objective: X-linked adrenal hypoplasia congenita (AHC) is characterized by primary adrenal insufficiency caused by deletion or mutation of the DAX-1 gene and is frequently associated with hypogonadotropic hypogonadism. It ...