عناصر مشابهة

• Identification of Novel Disease-Causing Gene Mutations Detected by Whole-Exome Sequencing and Whole - Genome Sequencing in Palestinian Families with Rare Diseases
  بواسطة: Alshaer, Shurouq Abdullah Yaghnam منشور: (2022)
• New SCN1A Mutation in Libyan Nonidentical Twin
  بواسطة: Assaleh, Yousef A. منشور: (2015)
• Genetic Analysis of Six Families Affected With Hereditary Spastic Paraplegia HSP
  بواسطة: Al-Salmi, Fatema Abdullah منشور: (2013)
• Characterisation of Mutation Causing type 1 Von Willebrand Disease
  بواسطة: Al Buhairan, Ahlam Mubarak منشور: (2004)
• Identification and Characterization of Mutations in Genes Implicated in Familial Hyperchlosterolaemia in Omani Families
  بواسطة: Al-Zidi, Ward Al-Muna Ali Rashid منشور: (2013)