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)
• 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)
• A Study of Cathepsin C Gene Mutations in Saudi Population with Papillon-Lefevre Syndrome
  بواسطة: Sharaf, Hanaa I. منشور: (2009)
• Inheritance of Resistance to Powdery Mildew Disease in Cucumber (Cucumis sativus L.)
  بواسطة: Ahmad, Nabil Moh'd Deeb منشور: (1994)
• Studies On Enzootic - Muscular Dystrophy In Lambs - stiff - lamb Disease -
  بواسطة: Ismail, Ismail Khalifa منشور: (1982)