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A rare genetic defect of MBL2 increased the risk for progression of IgA nephropathy
Ehlers-Danlos Syndrome is associated with Idiopathic Urticaria–a Retrospective Study
Relationship among ETV1 genetic polymorphisms, PFS, and microRNA in gastrointestinal stromal tumors.
Common Genetic Variations Associated with the Persistence of Immunity following Childhood Immunization
Genetic polymorphisms in Sox17 associated with intracranial aneurysm in Chinese Han people: a genotype-phenotype study
Association of three candidate genetic variants in ACMSD/TMEM163, GPNMB and BCKDK/STX1B with sporadic Parkinson’s disease in Han Chinese
Genetic susceptibility of common polymorphisms in NIN and SIGLEC5 to chronic periodontitis
IL‐4 gene polymorphisms and their relation to steroid‐induced osteonecrosis of the femoral head in Chinese population
3′ UTR variants of TNS3, PHLDB1, NTN4, and GNG2 genes are associated with IgA nephropathy risk in Chinese Han population
Genetic variants in the ITPR2 gene are associated with Kashin‐Beck Disease in Tibetan