Molecular pathogenesis of congenital adrenal hyperlasia (21-haydroxylase deficiency) and x-linked adrenal hypoplasia congenita /

مواد مشابهة

• Congenital adrenal hyperplasia in Malaysian paediatric endocrine tertiary centre : a review of cases and growth outcome /
  بواسطة: Nurmaira Hashim
  منشور في: (2017)
• Adrenal insufficiency in acute coronary syndrome /
  بواسطة: Norasyikin A. Wahab
  منشور في: (2005)
• Adrenal insufficiency in nephrotic syndrome children on corticosteroid treatment /
  بواسطة: Khairunnisa Mohamad Khalil
  منشور في: (2018)
• Software based prediction of structural and functional defects of 21-alpha hydroxylase enzyme mutations linked to congenital adrenal hyperplasia /
  بواسطة: Alirezaie, Najmeh Sadaat
  منشور في: (2011)
• Congenital hypothyroidism: demographic features, clinical pesentation and neurodevelopmental outcome /
  بواسطة: Sabeera Begum Kader Ibrahim
  منشور في: (2001)