4

عناصر مشابهة

• Identification and Characterization of Mutations in Genes Implicated in Familial Hyperchlosterolaemia in Omani Families
  بواسطة: Al-Zidi, Ward Al-Muna Ali Rashid منشور: (2013)
• Genetic Characterization of Hemoglobin S-Oman: A Severe Dominant Form of Sickle Cell Disease
  بواسطة: Al Hosni, Asisha Salim منشور: (2016)
• Homozygosity Mapping of Corneal Dystrophy in an Omani Family
  بواسطة: Al-Qasmi, Fatma Said منشور: (2011)
• Genetic Analysis of Six Families Affected With Hereditary Spastic Paraplegia HSP
  بواسطة: Al-Salmi, Fatema Abdullah منشور: (2013)
• A Study of the Genetic Causes of Progressive Myoclonic Epilepsy Cases in Six Families From Oman
  بواسطة: Al-Habsi, Muna Mohamed منشور: (2013)