15

عناصر مشابهة

• THE ROLE OF A SPLICE SITE MUTATION OF TIMP3 IN THE INHERITED EYE DISEASE SORSBY’S FUNDUS DYSTROPH
  بواسطة: Al Saffar, Fatimah منشور: (2011)
• New SCN1A Mutation in Libyan Nonidentical Twin
  بواسطة: Assaleh, Yousef A. منشور: (2015)
• Genomic Analysis of inherited Melanoma in a Palestinian Family: A Next Generation Sequencing Study
  بواسطة: Mohammad, Eman Fares منشور: (2022)
• L-2-Hydroxyglutaric Aciduria in Two Palestinian Siblings with a Novel Mutation in the L2HGDH Gene
  بواسطة: دويكات، عماد منشور: (2024)
• Characterisation of Mutation Causing type 1 Von Willebrand Disease
  بواسطة: Al Buhairan, Ahlam Mubarak منشور: (2004)