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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)
• Ultrastructure and Molecular Abnormalities in Cilia of the Respiratory System Leading to Primary Ciliary Dyskinesia in Omani Patients
  بواسطة: Al Adawi, Kawther Mohammed منشور: (2023)
• Patterns of Mutations among Treatment-Naïve and Treatment-Experienced Patients with Chronic HBV Infection in Jordan
  بواسطة: أبو خضرة، هيا محمد عبدالرحمن منشور: (2021)
• Methylenetetrahydrofolate Reductase (MTHFR) Gene Polymorphisms as Risk Factors for Down Syndrome in Jordan
  بواسطة: Al Refai, Ekhlas Ahmad Mohammed منشور: (2006)
• L-2-Hydroxyglutaric Aciduria in Two Palestinian Siblings with a Novel Mutation in the L2HGDH Gene
  بواسطة: دويكات، عماد منشور: (2024)