Yazar "Aydın M." 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 ... -
New features for child metrics: Further growth references and blood pressure calculations
Demir K.; Konakçı E.; Özkaya G.; Demir B.K.; Özen S.; Aydın M.; Darendeliler F. (Galenos Yayincilik,, 2020)Many new features have recently been incorporated to ÇEDD Çözüm/Child Metrics, an online and freely accessible scientific toolset. Various auxological assessments can now be made with data of children with genetic diseases ...
