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The RAD51C exonic splice-site mutations c. 404G> C and c. 404G> T are associated with familial breast and ovarian cancer
Mutation detection for biochemical genetics in the genomic era
Vitamin B12 deficiency in inflammatory bowel disease: a prospective observational pilot study
Validation analysis of known hypermethylated genes in cervical carcinoma at high-risk population
Replicative Analysis Of 30 Snps In Russian Patients With Alzheimer’s Disease
Damaging Missense De Novo Coding Mutations Contribute To Schizophrenia Risk
Polymorphisms in CYP2C8 and CYP3A5 genes in the Nigerian population
Genetic variation in Kruppel like factor 15 is associated with left ventricular hypertrophy in patients with type 2 diabetes: discovery and replication cohorts
Impacts of different cytokine and chemokine polymorphisms in Pakistani asthmatics a case control study
Association of common polymorphisms with gestational diabetes mellitus in Japanese women: A case-control study