عناصر مشابهة

• Pre-implantation Genetic Diagnosis PGD in Saudi Arabia : Should it be implemented as a routine method to prevent haemoglobinopathies
  بواسطة: Al Ghuwainem, Ghannimah Youssef منشور: (2011)
• 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 Role of Mutations in Timp-3 in the Inherited eye disease, Sorsbys fundus dystrophy
  بواسطة: Mujamammi, Ahmed Hussaim منشور: (2009)
• Prevalence of Primary Hypercholesterolemia among Gulf People and Preliminary Study of LDL-R Mutations in a Sample of Gulf Citizens with Familial Hypercholesterolemia
  بواسطة: Al Bati, Neda Ali Hassan منشور: (2007)
• A STUDY OF THE RELATIONSHIP BETWEEN ABCA I GENE POLYMORPHISMS, PLASMA LIPID LEVELS AND RISK OF ATHEROSCLEROSIS.
  بواسطة: Bogari, Neda Mustafa منشور: (2007)