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LPHN3 gene variations and susceptibility to ADHD in Chinese Han population: a two-stage case–control association study and gene–environment interactions
Influence of CTNNB1 rs2953 polymorphism on schizophrenia susceptibility in Chinese Han population through modifying miR‐485 binding to CTNNB1
A multiethnic meta-analysis defined the association of rs12946942 with severe adolescent idiopathic scoliosis
Oxytocin receptor gene (OXTR) and father support interact to predict depressive symptoms postpartum
Genetic ancestry analysis reveals misclassification of commonly used cancer cell lines
Genomic Analysis of Circulating Tumor DNA Using a Melanoma-Specific UltraSEEK Oncogene Panel
FKBP1A rs6041749 polymorphism is associated with allograft function in renal transplant patients
Comparison between MassARRAY and pyrosequencing for CYP2C19 and ABCB1 gene variants of clopidogrel efficiency genotyping
MTHFR gene specific and global methylation patterns in normal pregnancy: A pilot study (India)
A Functional Variant in Ubiquitin Conjugating Enzyme E2 L3 Contributes to Hepatitis B Virus Infection and Maintains Covalently Closed Circular DNA Stability by Inducing Degradation of Apolipoprotein B mRNA Editing Enzyme Catalytic Subunit 3A
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