عناصر مشابهة

• ROLES OF KRÜPPEL LIKE FACTORS KLF1, KLF2, AND KLF4 IN EMBRYONIC BETA-GLOBIN GENE EXPRESSION
  بواسطة: Al Hashem, Yousef Nassir منشور: (2009)
• Characterization of novel mutation in the upstream promoter of the F2R gene in a patient with type 1 von Willebrand disease
  بواسطة: Sabi, Essa M. منشور: (2011)
• The Study of the Relationship between the Null Genotype of GSTM1 and GSTT1 Genes and Diabetic Nephropathy in Thi-Qar Province
  بواسطة: فيصل، هدى طاهر منشور: (2014)
• Screening polycythemia vera and essential thrombocythemia patients for JAK2 and c-KIT genetic mutations
  بواسطة: Al Shaka'a, Hind Riad Adel منشور: (2008)
• Screening for 3.7 and 4.2 Deletion Mutations in Sudanese Patients Suspected to Alpha Thalassaemia
  بواسطة: Balloula, Hussam Ali Osman منشور: (2017)