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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
Physical activity and sedentary behavior can modulate the effect of the PNPLA3 variant on childhood NAFLD: a case-control study in a Chinese population
ZNF208 polymorphisms associate with ischemic stroke in southern Chinese Han population
Polymorphisms of ABAT, SCN2A and ALDH5A1 may affect valproic acid responses in the treatment of epilepsy in Chinese
Revealing hidden species diversity in closely related species using nuclear SNPs, SSRs and DNA sequences – a case study in the tree genus Milicia