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)
• Non-Syndromic Autosomal Recessive Deafness in Gaza Strip: A Study on Selected Connexin 26 Gene Mutations
  بواسطة: Essammak, Badria F. منشور: (2014)
• 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)
• The Association Between Angiotensin 11 Type 1 Receptor Gene Atir A1166c Variants and Essential Hypertension in A Sample of The Jordanian Population
  بواسطة: Shahin, Dima Shahin Ali منشور: (2012)