Article

ASSESSMENT OF THE SIGNIFICANCE OF POLYMORPHISM WNT3 GENE IN ANOMALIES OF FETUS DEVELOPMENT IN PREGNANT WOMEN OF THE SAMARKAND POPULATION

Eltazarova Gulnara Sherbekovna PhDSamarkand State Medical UniversityKhudoyarova Dildora Rakhimovna DS d.m.s.Head of the Department of Obstetrics and Gynecology No. 1 Samarkand State Medical University

Zenodo (CERN European Organization for Nuclear Research)repository2022en

ABI

Abstract

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.

Topics

Hermeneutics and Narrative Identity Aging, Elder Care, and Social Issues Health, Medicine and Society

Identifiers

DOI: 10.5281/zenodo.6619476

Citations and references

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