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)
• Identification of Mutations That Cause Congenital Insensitivity to Pain in Affected Palestinian Families
  بواسطة: Khaled, Boushra منشور: (2022)
• Detection of 185 delAG Mutation in Breast Cancer 1 BRCA1 Gene Among Libyan Women Attending Breast Cilinc
  بواسطة: Essarbout, Amel A. منشور: (2012)
• Hybrid Mutations : Performance Studies as a Generative force in Contemporary Theatre
  بواسطة: Harvey, Hannah B. منشور: (2009)