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Genetic diversity of 71 Y-chromosomal biallelic markers in the Han population living in Southern China
Childhood-onset Leigh syndrome transforming into an episodic weakness phenotype with axonal neuropathy caused by MT-ATP6 mutations
The RAD51C exonic splice-site mutations c. 404G> C and c. 404G> T are associated with familial breast and ovarian cancer
Replicative Analysis Of 30 Snps In Russian Patients With Alzheimer’s Disease
Damaging Missense De Novo Coding Mutations Contribute To Schizophrenia Risk
Association of polymorphism in the dopamine receptors and transporter genes with hyperprolactinemia in patients with schizophrenia
Role of rs1501299 variant in the adiponectin gene on total adiponectin levels, insulin resistance and weight loss after a Mediterranean hypocaloric diet
Association of transketolase polymorphisms with measures of polyneuropathy in patients with recently diagnosed diabetes
Association between Cullin-3 single-nucleotide polymorphism rs17479770 and essential hypertension in the male Chinese Han population
Association between Two Resistin Gene Polymorphisms and Metabolic Syndrome in Jilin, Northeast China: A Case-Control Study