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)
• Molecular Investigations in Chronic Myeloid Leukemia : Monitoring Residual Disease and Screening for BCR-ABL Mutations
  بواسطة: Al Yami, Nasher Hussein Al Sedran منشور: (2008)
• Von Willebrand Factor Gene Exon 28 Polymorphisms and Phenotypic Characteristics in Sickle Cell Disease in Eastern Saudi Arabia
  بواسطة: اليامي، فاطمه سالم عايض منشور: (2020)
• Prevalence of BRCAI 185delAG, BTCA1 5382insC and BRCA2 6174delT mutations and their association with breast cancer in Jordanian females
  بواسطة: Al Yosef, Hussein M. منشور: (2015)
• 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)