- Assessment of the Implementation of Pharmacogenomic Testing in a Pediatric Tertiary Care Setting
- A validation study of the UGT1A4 rs2011404 variant and the risk of anti‐tuberculosis drug‐induced hepatotoxicity in an Eastern Chinese Han population
- Moderating Role of TSHR and PTPN22 Gene Polymorphisms in Effects of Excessive Fluoride on Thyroid: a School-Based Cross-Sectional Study
- Hemodialysis-Related Glycemic Disarray Proven by Continuous Glucose Monitoring: Glycemic Markers and Hypoglycemia
- Variation in biomarker levels of metals, persistent organic pollutants, and omega-3 fatty acids in association with genetic polymorphisms among Inuit in Nunavik, Canada
- Correlation between TGF-β2/3 promoter DNA methylation and Smad signaling during palatal fusion induced by 2, 3, 7, 8-tetrachlorodibenzo-p-dioxin
- Identification of the PmWEEP locus controlling weeping traits in Prunus mume through an integrated genome-wide association study and quantitative trait locus mapping
- The Association of Vitamin D and Gene Variants in the Vitamin D Metabolic Pathway with Preterm Birth
- (Re-)activity in the caregiving situation: Genetic diversity within Oxytocin–Vasopressin Pathway is associated with salivary oxytocin and vasopressin concentrations in response to contact with a crying infant-simulator
- Detection of Cryptic Fragile X Full Mutation Alleles by Southern Blot in a Female and Her Foetal DNA via Chorionic Villus Sampling, Complicated by Mosaicism for 45,X0/46,XX/47,XXX
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