6

عناصر مشابهة

• Genetic Analysis of Six Families Affected With Hereditary Spastic Paraplegia HSP
  بواسطة: Al-Salmi, Fatema Abdullah منشور: (2013)
• Mutation Analysis of the Non-Syndromic Autosomal Recessive Deafness (NSARD) Associated Otoferlin Gene: A Study on Omani Patients Using Bioinformatic Analyses
  بواسطة: Hamza, Nishath منشور: (2004)
• Molecular Cytogenetic Analysis of Telomeres in Cells with Mutant Brca1 and Brca2 Genes
  بواسطة: Al Wahiby, Suliman Abd Allah A. منشور: (2005)
• Identification and Characterization of Mutations in Genes Implicated in Familial Hyperchlosterolaemia in Omani Families
  بواسطة: Al-Zidi, Ward Al-Muna Ali Rashid منشور: (2013)
• The Analysis of CACNA1D as A Candidate Gene for Heart Pacemaker Control in Oman Family Study
  بواسطة: Al-Anbouri, Lamyaa Hamood منشور: (2010)