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Association of Single-Nucleotide Polymorphism REX1 rs6815391, OCT4 rs13409 or rs3130932, and CTBP2 rs3740535 with Primary Lung Cancer Susceptibility: A Case-Control Study in a Chinese Population
Novel non-synonymous mutations of PAX8 in a cohort of Chinese with congenital hypothyroidism
Associations between UGT2B7 polymorphisms and cancer susceptibility: A meta-analysis
Evaluation of significant genome-wide association studies risk—SNPs in young breast cancer patients
Beta2-Adrenergic Receptor Polymorphisms and Haplotypes Associate With Chronic Pain in Sickle Cell Disease
Dataset of allele, genotype and haplotype frequencies of four LIN28B gene polymorphisms analyzed for association with age at menarche in Russian women
Correlation of EYS polymorphisms with lumbar disc herniation risk among Han Chinese population
A functional variant of CB2 receptor gene interacts with childhood trauma and FAAH gene on anxious and depressive phenotypes
CHRNA5/CHRNA3 gene cluster is a risk factor for lumbar disc herniation: a case-control study
Sequence variants in FSHR and CYP19A1 genes and the ovarian response to controlled ovarian stimulation