Keywords
WNT3 gene, polymorphism, gene, alleles, genotype, fetal abnormalities, pregnancy, fetus, genome-wide association search (GWAS).
Abstract
In practical health care around the world, the problem of studying congenital malformations and / or hereditary diseases is a very relevant medical and social problem in view of the main disability and mortality of both children and adults. According to research, the root cause of the development of fetal anomalies are genetic factors that lead to a violation of the control of the process of cell division.