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Accurate detection of low prevalence AKT1 E17K mutation in tissue or plasma from advanced cancer patients
ACE GENE VARIANTS AND SARCOIDOSIS IN A FINNISH POPULATION
Acid-free glyoxal as a substitute of formalin for structural and molecular preservation in tissue samples
A Genome-wide Association Study of Dupuytren Disease Reveals 17 Additional Variants Implicated in Fibrosis
Adenosquamous gallbladder carcinoma: multigene hotspot mutational profiling reveals a monoclonal origin of the two components
A missense mutation in damage specific DNA binding protein 2 is a genetic risk factor for limbal squamous cell carcinoma in horses
Adrenergic Receptor Genotypes Influence Post-operative Outcomes in Infants in the Single Ventricle Reconstruction Trial
A New Targeted CFTR Mutation Panel Based on Next-Generation Sequencing Technology
Age at menarche and cardiovascular risk factors using Mendelian randomization in the Guangzhou Biobank Cohort Study
A Novel Variant with Positive Natural Selection Influenced Hb A2 Levels in Chinese Individuals with ?-Thalassemia