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عناصر مشابهة

• Screening of the Arabic Allele and Putative Mutations in Exons 4 and 17 of LDLR and in Exon 26 of Apob100 in 100 Kuwaiti Patients with Coronary Heart Disease or Hypercholesterolemia
  بواسطة: بوخماس، هناء يوسف عيد منشور: (2014)
• Screening Mutations in the Low Density Lipoprotein Receptor Gene Responsible for Familial Hypercholesterolemia in Jordanian Patients
  بواسطة: Al Dasouqi, Omran Hussein منشور: (2003)
• Prevalence of Primary Hypercholesterolemia among Gulf People and Preliminary Study of LDL-R Mutations in a Sample of Gulf Citizens with Familial Hypercholesterolemia
  بواسطة: Al Bati, Neda Ali Hassan منشور: (2007)
• The Role of Factor V Leiden and Prothrombin G20210A Mutations in the Hypercoagulable State Associated with Ischaemic Stroke among Sudanese Patients
  بواسطة: Ahmed, Elshazali Widaa Ali Mohamed منشور: (2012)
• Mutation Analysis of the Low Density Lipoprotein Receptor Gene in Clinically Diagnosed Arab Family with Familial Hypercholesterolemia
  بواسطة: القلاف، هالة ماجد سلطان منشور: (2011)