عناصر مشابهة

• STUDY ON G6PD DEFICIENCY IN UNEXPLAINED NEONATAL JAUNDICE
  بواسطة: MOSHIRA ABD EL - ZAHER ABD EL - MAKSOUD منشور: (2011)
• EVALUATION OF THE ROLE OF G6PD DEFICIENCY AND ABO INCOMPATIBILITY IN NEONATAL JAUNDICE
  بواسطة: MONA SALAH EL DIN FARRAG منشور: (1995)
• Gene mutation and qualitative enzyme assay of G٦PD enzyme deficiency in neonatal hyperbilirubinemia
  بواسطة: Othman Rizk Abdelmeguid Mishref منشور: (2012)
• A Reviewon G-6-PD Deficiency In Relation To Sickle Cellanaemia 
  بواسطة: Hamid:Hamid Ahmed  منشور: (1986)
• G6PD gene polymorphisms in Egytian deficient patients
  بواسطة: Omnia Yahia Ibrahim Abdeldayem منشور: (2012)