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  • Molecular diagnosis of severe combined immunodeficiency using whole-exome sequencing
  • DNA Hypermethylation Mediated Downregulation of Antioxidant Genes in Early Onset of Cataract in High Myopic Eyes
  • P133 HLA-ANTIGENS and disease manifestation in a cohort of 600 southern french patients with psoriatic arthritis
  • Association of TPH2 gene polymorphism with response to antidepressant treatment among ethnic Han Chinese population
  • No association of GRIN2A polymorphisms with the major depressive disorder in the Chinese Han origin
  • RelationshipbetweenHTRA1 polymorphism and genetic susceptibility of wet age-related macular degeneration in Han population
  • Gene variants in the folate pathway are associated with increased levels of folate receptor autoantibodies
  • The interaction between BRAF mutation and microsatellite instability (MSI) status in determining survival outcomes after adjuvant 5FU based chemotherapy in stage …
  • The common VWF single nucleotide variants c. 2365A> G and c. 2385T> C modify VWF biosynthesis and clearance
  • No association between the vitamin D pathway gene polymorphisms and bone biomarkers response to calcium and low dose calcitriol supplementation in …
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