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)
• L-2-Hydroxyglutaric Aciduria in Two Palestinian Siblings with a Novel Mutation in the L2HGDH Gene
  بواسطة: دويكات، عماد منشور: (2024)
• Genetic Analysis of Six Families Affected With Hereditary Spastic Paraplegia HSP
  بواسطة: Al-Salmi, Fatema Abdullah منشور: (2013)
• New SCN1A Mutation in Libyan Nonidentical Twin
  بواسطة: Assaleh, Yousef A. منشور: (2015)
• Characterisation of Mutation Causing type 1 Von Willebrand Disease
  بواسطة: Al Buhairan, Ahlam Mubarak منشور: (2004)