Associated Papers
Significant Associations between AXIN1 rs1805105, rs12921862, rs370681 Haplotypes and Variant Genotypes of AXIN2 rs2240308 with Risk of Congenital Heart Defects.
Crauciuc GA et al.
International Journal of Environmental Research and Public Health, 2020
Novel mutations of AXIN2 identified in a Chinese Congenital Heart Disease Cohort.
Zhu MJ et al.
Journal of Human Genetics, 2019
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