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Relationship between glucose homeostasis and obesity in early life—A study of Italian children and adolescents
Variation in the vitamin D receptor gene, plasma 25-hydroxyvitamin D, and risk of premenstrual symptoms
Nuclear Pore Glycoprotein 62 Genetic Variant rs9523 is Associated with Clinical Outcomes of Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitors in Lung Adenocarcinoma Patients
The combined effects of nucleotide-binding domain-like receptor protein 3 polymorphisms and levels of blood lead on developmental delays in preschool children NLRP3, lead, arsenic and developmental delay
A Common Variant in 11q23.3 Is Associated with Susceptibility to Atopic Dermatitis in the Han Chinese Population
Steroid profiling and genetic variants in Chinese women with gestational diabetes mellitus
A single nucleotide polymorphism in the IL1RL1 gene is associated with Behcet’s disease in a Chinese Han population
The Effects of Gene Variations of GABRA2, GABRB1, GABRG2, GAD1 and SLC1A3 on Patients with Propofol During Anesthesia Induction
Preliminary study of genome-wide association identified novel susceptibility genes for thyroid-related hormones in Chinese population
Novel FCN2 Variants and Haplotypes are Associated with Rheumatic Heart Disease
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