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عناصر مشابهة

• Genetics of Wilson Disease in Omani Families
  بواسطة: Al-Tobi, Mohammed Nasser Rashid منشور: (2007)
• Identification and Characterization of Mutations in Genes Implicated in Familial Hyperchlosterolaemia in Omani Families
  بواسطة: Al-Zidi, Ward Al-Muna Ali Rashid منشور: (2013)
• Analysis of Polymorphisms in Three Different Genes in Relation to Blood Pressure Phenotypes in Omani From Nizwa District
  بواسطة: Al-Lawati, Fatma منشور: (2006)
• Assay Development for the Detection of FGF23 Mutations That Cause Familial Tumoral Calcinosis by Amplification Refractory Mutation System (ARMS)
  بواسطة: الغامدي، منال عبدالله سعيد منشور: (2011)
• Autozygosity Mapping of Two Molecularly Uncharacterized Autosomal Recessive Genetic Conditions Achalalasia and Ataxia-Epilepsy in Two Consanguineous Omani Families
  بواسطة: Al-Yarubi, Naeema Soud Said منشور: (2015)