All Stories

  1. Assessment of Six Polymorphic Variants as Genetic Risks for Coronary Artery Disease: A Case–Control Study
  2. Congenital Anomalies in Neonates: Findings from Six Baghdad Hospitals
  3. Spectrum and classification ofATP7Bvariants with clinical correlation in children with Wilson disease
  4. Epigenomic and phenotypic characterization of DEGCAGS syndrome
  5. Molecular detection of mononucleotide biomarkers of microsatellite instability in sporadic colorectal carcinoma patients with clinicopathological correlation
  6. Molecular Analysis of CYP21A2 Gene Mutations among Congenital Adrenal Hyperplasia Patients in Iraq
  7. Molecular analysis of CFTR gene mutations among Iraqi cystic fibrosis patients
  8. Impact of JAK2 mutation on clinical and hematological parameters of myeloproliferative neoplasms.
  9. Rare inherited syndrome
  10. Molecular Analysis ofCYP21A2Gene Mutations among Iraqi Patients with Congenital Adrenal Hyperplasia
  11. Association of Higher Defensin β-4 Genomic Copy Numbers with Behçet’s Disease in Iraqi Patients
  12. The Spectrum of β-Thalassemia Mutations in Baghdad, Central Iraq
  13. Molecular characterization of glucose-6-phosphate dehydrogenase deficient variants in Baghdad city - Iraq