عناصر مشابهة

• 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)
• RAPID SCREENING OF BCR/ABL FUSION TRANSCRIPTS IN PHILADELPHIA CHROMOSOME POSITIVE LEUKEMIAS BY MULTIPLEX RT-PCR
  بواسطة: Akkawi, Nadia Awni منشور: (2005)
• Biochemical Basis of Dasatnib Resistance in Chronic Myeloid Leukemia
  بواسطة: Baty, Roua منشور: (2011)