عناصر مشابهة

• 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)
• Interindividual variation in aflatoxin B1 exposure and the concomitent polymorphisms of certain 450s among Jordanian population
  بواسطة: Salameh, Ghada Abd Almajeed منشور: (2010)
• Characterisation of Mutation Causing type 1 Von Willebrand Disease
  بواسطة: Al Buhairan, Ahlam Mubarak منشور: (2004)
• THE ROLE OF A SPLICE SITE MUTATION OF TIMP3 IN THE INHERITED EYE DISEASE SORSBY’S FUNDUS DYSTROPH
  بواسطة: Al Saffar, Fatimah منشور: (2011)
• Screening mutations in the low density lipoprotein receptor gene responsible for familial Hypercholesterolemia in Jordanian patients
  بواسطة: Al Dasouqi, Omran Hussein منشور: (2003)