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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)
• THE ROLE OF A SPLICE SITE MUTATION OF TIMP3 IN THE INHERITED EYE DISEASE SORSBY’S FUNDUS DYSTROPH
  بواسطة: Al Saffar, Fatimah منشور: (2011)
• Next Generation Sequencing And The Population Genomics of Yeast
  بواسطة: Al Harbi, Sultan Nafea A. منشور: (2012)
• Hybrid Mutations : Performance Studies as a Generative force in Contemporary Theatre
  بواسطة: Harvey, Hannah B. منشور: (2009)
• Identification of Mutations That Cause Congenital Insensitivity to Pain in Affected Palestinian Families
  بواسطة: Khaled, Boushra منشور: (2022)