عناصر مشابهة

• Mutation Analysis of the Low Density Lipoprotein Receptor Gene in Clinically Diagnosed Arab Family with Familial Hypercholesterolemia
  بواسطة: القلاف، هالة ماجد سلطان منشور: (2011)
• Identification and Characterization of Mutations in Genes Implicated in Familial Hyperchlosterolaemia in Omani Families
  بواسطة: Al-Zidi, Ward Al-Muna Ali Rashid منشور: (2013)
• Identification of low density lipoprotein receptor gene mutations in patients suffring from familial hypercholestolemia disease in Jordan
  بواسطة: محيسن، سميرة خضر منشور: (2010)
• Screening for MSX1 and PAX9 Gene Mutations among Hypodontia Patients in Jordanian Population
  بواسطة: القرعان، أريج محمد منشور: (2022)
• Screening for mutations in B-cardiac myosin heavy chain gene among Jordanian patients with familial hypertrophic cardiomyopathy.
  بواسطة: Habbab, Wesal Marwan منشور: (2007)