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High-throughput detection of common sequence variations of Fabry disease in Taiwan using DNA mass spectrometry
Hypoxia-inducible factor-1? gene polymorphisms in early and late onset preeclampsia in Sinhalese women
Identification and validation of loss of function variants in clinical contexts
Identification of a New Target of miR-16, Vacuolar Protein Sorting 4a
Genetic variation at the CYP2C19 gene associated with metabolic syndrome susceptibility in a South Portuguese population: results from the pilot study of the European Health Examination Survey in Portugal
Genetic Variation in FADS Has Little Effect on the Association between Dietary PUFA Intake and Cardiovascular Disease
Genetic variation in microRNA-binding site and prognosis of patients with colorectal cancer
Genetic variations in SLC3A2/CD98 gene as prognosis predictors in non-small cell lung cancer
Genetic Variations in STK11, PRKAA1, and TSC1 Associated with Prognosis for Patients with Colorectal Cancer
Genetic variations of MMP9 gene and intracerebral hemorrhage outcome: A cohort study in Chinese Han population