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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
Hemodialysis-Related Glycemic Disarray Proven by Continuous Glucose Monitoring: Glycemic Markers and Hypoglycemia
EYA2 suppresses the progression of hepatocellular carcinoma via SOCS3-mediated blockade of JAK/STAT signaling
Variation in biomarker levels of metals, persistent organic pollutants, and omega-3 fatty acids in association with genetic polymorphisms among Inuit in Nunavik, Canada
Real-world data on treatment outcomes in EGFR-mutant non-small-cell lung cancer patients receiving osimertinib in second or further lines
GJA1 rs2071165 A> G Variant Increased Gastric Cancer Risk in Females of Northwest China: A Case-Control Study
Contribution of lncRNA CASC8, CASC11 and PVT1 genetic variants to the susceptibility of coronary heart disease
Impact of COL6A4P2 gene polymorphisms on the risk of lung cancer: A case-control study
Genetic Analysis in a Taiwanese Cohort of 750 Index Patients with Clinically Diagnosed Familial Hypercholesterolemia
Association of vitamin D receptor polymorphisms with metabolic syndrome‐related components: A cross‐sectional study
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