عناصر مشابهة

• Assay Development for the Detection of FGF23 Mutations That Cause Familial Tumoral Calcinosis by Amplification Refractory Mutation System (ARMS)
  بواسطة: الغامدي، منال عبدالله سعيد منشور: (2011)
• Assay Development for the Detection of FGF23 Mutations That Cause Familial Tumoral Calcinosis by Amplification Refractory Mutation System (ARMS)
  بواسطة: Al Ghamdi, Manal Abd Allah S. منشور: (2011)
• 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)
• Hybrid Mutations : Performance Studies as a Generative force in Contemporary Theatre
  بواسطة: Harvey, Hannah B. منشور: (2009)