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Search Results for: Hereditary Genetics
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Variants in RETN gene are associated with steroid-induced osteonecrosis of the femoral head risk among Han Chinese people.
Association of heme oxygenase-1 single nucleotide polymorphisms with susceptibility to tuberculosis in Chinese Han population.
Genetic variants in RET, ARHGEF3 and CTNNAL1, and relevant interaction networks, contribute to the risk of Hirschsprung disease.
Primary qualities evoked by quinine, sucrose, and capsaicin associate with PROP bitterness, but not TAS2R38 genotype
A New Risk Variant for Multiple Sclerosis at 11q23.3 Locus Is Associated with Expansion of CXCR5+ Circulating Regulatory T Cells
Intracranial aneurysm’s association with genetic variants, transcription abnormality, and methylation changes in ADAMTS genes
The association between the rs4987105 of 5-lipoxygenase (ALOX5) gene and gestational glucose metabolism in Chinese population.
Association of Serum Uric Acid with Metabolic Syndrome and Its Components: A Mendelian Randomization Analysis
Association of EPAS1 and PPARA Gene Polymorphisms with High-Altitude Headache in Chinese Han Population
GWAS for time to failure of kidney transplants from African American deceased donors
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