2

عناصر مشابهة

• Screening Mutations in the Low Density Lipoprotein Receptor Gene Responsible for Familial Hypercholesterolemia in Jordanian Patients
  بواسطة: Al Dasouqi, Omran Hussein منشور: (2003)
• Genetics of Wilson Disease in Omani Families
  بواسطة: Al-Tobi, Mohammed Nasser Rashid منشور: (2007)
• Mutation Analysis of the Low Density Lipoprotein Receptor Gene in Clinically Diagnosed Arab Family with Familial Hypercholesterolemia
  بواسطة: القلاف، هالة ماجد سلطان منشور: (2011)
• Genetic Analysis of Six Families Affected With Hereditary Spastic Paraplegia HSP
  بواسطة: Al-Salmi, Fatema Abdullah منشور: (2013)
• 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)