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)
• 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)
• The Influence of Disease Modifying Mutations in Related Metabolie Pathways for Nucleotides : Mutations in Nucleotidase Genes Affecting Nuclear and Mitochondrial DNA
  بواسطة: Zamaami, Mazin Abd Alaziz Abd Alhadi منشور: (2012)
• Screening mutations in the low density lipoprotein receptor gene responsible for familial Hypercholesterolemia in Jordanian patients
  بواسطة: Al Dasouqi, Omran Hussein منشور: (2003)