عناصر مشابهة

• THE ROLE OF A SPLICE SITE MUTATION OF TIMP3 IN THE INHERITED EYE DISEASE SORSBY’S FUNDUS DYSTROPH
  بواسطة: Al Saffar, Fatimah منشور: (2011)
• A Study of Cathepsin C Gene Mutations in Saudi Population with Papillon-Lefevre Syndrome
  بواسطة: Sharaf, Hanaa I. منشور: (2009)
• Characterization of novel mutation in the upstream promoter of the F2R gene in a patient with type 1 von Willebrand disease
  بواسطة: Sabi, Essa M. منشور: (2011)
• Identification of low density lipoprotein receptor gene mutations in patients suffring from familial hypercholestolemia disease in Jordan
  بواسطة: Mhasien, Sameera Khader منشور: (2010)
• Indentification of Cystic Fibrosis Mutations Among Jordanian Patients
  بواسطة: فريحات، عبير عبدالغفار منشور: (2007)