عناصر مشابهة

• Screening Mutations in the Low Density Lipoprotein Receptor Gene Responsible for Familial Hypercholesterolemia in Jordanian Patients
  بواسطة: Al Dasouqi, Omran Hussein منشور: (2003)
• SCREENING FOR SC1 AS CANDIDATE GENE AMONG BEHCET'S DISEASE JORDNAIAN PATIENTS
  بواسطة: Abu Eshiekh, Hanan Rashid منشور: (2009)
• Screening for mutations in B-cardiac myosin heavy chain gene among Jordanian patients with familial hypertrophic cardiomyopathy.
  بواسطة: Habbab, Wesal Marwan منشور: (2007)
• Detection of Mutations and Polymorphisms of APC, K-ras and P53 genes in Endoscopic Colorectal lesions among Sudanese Patients
  بواسطة: Ali, Ashwag Mohammed Mukhtar منشور: (2010)
• The Relationship between Mitochondrial Gene Cytochrome C Oxidase Subunit III "COX3" Mutation and Male Infertility in Jordanian Population
  بواسطة: الصمادي، أسماء عيسى منشور: (2022)