17

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)
• Re-analysis of Exome Sequencing Data of Intellectual Disability samples: Yield and Benefits
  بواسطة: النبهانية، مريم بنت محمد بن عثمان منشور: (2017)
• Identification of Genes Potentially Involved in the Development of Autism in Selected Palestinian Families Using Whole Exome Sequencing
  بواسطة: Abadi, Eman Jawad منشور: (2023)
• Neurodevelopmental Disorders and the Role of Pharmacotherapy: Review and Update
  بواسطة: الجادري، اسيل منشور: (2020)
• Genomic Studies of Autosomal Recessive Epilepsies in Three Omani Consanguineous Families
  بواسطة: Basak, Saroma منشور: (2016)