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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)
• Correlation of Major Iron Metabolism Related-Genes Single Nucleotide Polymorphisms "SNPs" with Autism Spectrum Disorder "ASD" in Palestinian Patients
  بواسطة: Rabaya, Sabha Fahmi منشور: (2021)
• Exome Sequencing of Neurodevelopmental Disorders in 125 Omani Families: Diagnostic Yield and Candidate Genes
  بواسطة: الكاسبي، غالية منشور: (2022)
• ON MERGING SEQUENCING AND SCHEDULING THEORY WITH GENETIC ALGORITHMS TO SOLVE STOCHASTIC JOB SHOPS
  بواسطة: Al Harkan, Ibrahim M. منشور: (1997)
• Identification and Characterization of Mutations in Genes Implicated in Familial Hyperchlosterolaemia in Omani Families
  بواسطة: Al-Zidi, Ward Al-Muna Ali Rashid منشور: (2013)