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Cytokine Genetic Variants and Health-Related Quality of Life in Crohn’s Disease: An Exploratory Study
Cystic fibrosis presentation in del. F508 and p. Tyr109Glyfs compound heterozygote CFTR state: a case report
STX1A gene variations contribute to the susceptibility of children attention-deficit/hyperactivity disorder: a case–control association study
Genetic aspects of idiopathic paediatric uveitis and juvenile idiopathic arthritis associated uveitis in Chinese Han
Investigating the role of microRNA-27a gene polymorphisms and its interactive effect with risk factors in gastrointestinal cancers
Mutated ATP10B increases Parkinson’s disease risk by compromising lysosomal glucosylceramide export
Gadd45b mediates depressive-like role through DNA demethylation
LGALS3 promotes treatment resistance in glioblastoma and is associated with tumor risk and prognosis
Association of the MMP-9 polymorphism and ischemic stroke risk in southern Chinese Han population
Clinical and Molecular Differences between 4-Year-Old Monozygous Male Twins Mosaic for Normal, Premutation and Fragile X Full Mutation Alleles