The relationship of 211G to A mutation of uridine diphosphoglucuronosyl tranferase 1A1 gene and severe neonatal jaundice in Malaysian Chinese newborn infants /

مواد مشابهة

• Study of UDP-glucurunosyl transferase 1A1 gene mutation in severe neonatal jaundice in malay neonates /
  بواسطة: Azlin Ithnin
  منشور في: (2008)
• Risk factors associated with significant neonatal jaundice among newborns from Larut Matang & Selama District Delivered in Taiping Hospital /
  بواسطة: Nor Bizura Abdul Hamid
  منشور في: (2002)
• The efficacy of different type of phototherapy light devices for neonatal jaundice treatment /
  بواسطة: Mohammad Hanafi Ismail
  منشور في: (2020)
• Pre-Discharge Transcutaneous Bilirubinometer as a Tool in Identification of Infants at High Risk of Developing Significant Jaundice /
  بواسطة: Chong, Chooi Siang
  منشور في: (2015)
• Prediction of significant neonatal jaundice in babies with ABO incompatibility by cord blood tests /
  بواسطة: Farisyah Syakirah Mohd Zain
  منشور في: (2011)