12

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)
• Genomic Analysis of inherited Melanoma in a Palestinian Family: A Next Generation Sequencing Study
  بواسطة: Mohammad, Eman Fares منشور: (2022)
• New SCN1A Mutation in Libyan Nonidentical Twin
  بواسطة: Assaleh, Yousef A. منشور: (2015)
• Aminotrasferase (TAT) Gene Mutations Among Palestinian Tyrosinemia Type II Patients : An extended study
  بواسطة: ريماوى، نيقين منشور: (2018)
• Characterisation of Mutation Causing type 1 Von Willebrand Disease
  بواسطة: Al Buhairan, Ahlam Mubarak منشور: (2004)