Plasma protein expression profiles and PAX8 gene mutation(s) screening of patients with congenital hypothyroidism /

مواد مشابهة

• Congenital hypothyroidism: demographic features, clinical pesentation and neurodevelopmental outcome /
  بواسطة: Sabeera Begum Kader Ibrahim
  منشور في: (2001)
• Mutational analysis of genes encoding thyroid stimulating hormone receptor (TSHR) and thyroid transcription factor, FOXE1 in patients with congenital hypothyroidism /
  بواسطة: Maslinda Musa
  منشور في: (2006)
• Comparison between weekly vs daily dosing L-thyroxine for the treatment of hypothyroidism in Ramadan - a pilot randomized controlled trial /
  بواسطة: Nurul Aulia binti Zakaria
  منشور في: (2018)
• Indices of neonatal thyroid function in Brunei Darussalam and its application to newborn screening for congenital hypothyroidism /
  بواسطة: Abdul Majid Haji Abdul Rahman
  منشور في: (1994)
• Characterisation of the human thyroid peroxidase gene mutations (S) in patients with congenital dyshormonogenetic hypothyroidism /
  بواسطة: Lee, Ching Chin
  منشور في: (2013)