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Search Results for: Hereditary Genetics
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Association of toll-like receptor 10 polymorphisms with paediatric idiopathic uveitis in Han Chinese
High expression of FAM13A was associated with increasing the liver cirrhosis risk
Genetic Variants Flanking the FGF21 Gene Were Associated with Renal Function in Chinese Patients with Type 2 Diabetes
Identification of regulatory variants associated with genetic susceptibility to meningococcal disease
Infancy onset maltreatment and the development of suicide ideation: an investigation of moderation by oxytocin-related gene polymorphisms
Correlation between the DEPDC5 rs1012068 polymorphism and the risk of HBV-related hepatocellular carcinoma
β2-Adrenergic Receptor Gene Polymorphisms Are Associated with Cardiovascular Events But not All-Cause Mortality in Coronary Artery Disease Patients: A Meta-Analysis of Prospective Studies
IRF5 is required for bacterial clearance in human m1-polarized macrophages, and irf5 immune-mediated disease risk variants modulate this outcome
Polymorphisms in CLDN1 are associated with age and differentiation of triple-negative breast cancer patients
CDK6 3’UTR polymorphisms alter the susceptibility to cervical cancer among Uyghur females
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