Significant Associations between AXIN1 rs1805105, rs12921862, rs370681 Haplotypes and Variant Genotypes of AXIN2 rs2240308 with Risk of Congenital Heart Defects

This study aimed to investigate possible associations of the susceptibility to congenital heart defects (CHDs) with AXIN1 rs1805105, rs12921862 and rs370681 gene variants and haplotypes, and AXIN2 rs2240308 gene variant. Significant associations were identified for AXIN1 rs370681 and AXIN2 rs2240308...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Publicado no:Int J Environ Res Public Health
Main Authors: Crauciuc, George Andrei, Iancu, Mihaela, Olah, Peter, Tripon, Florin, Anciuc, Mădălina, Gozar, Liliana, Togănel, Rodica, Bănescu, Claudia
Formato: Artigo
Idioma:Inglês
Publicado em: MDPI 2020
Assuntos:
Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7589771/
https://ncbi.nlm.nih.gov/pubmed/33096676
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijerph17207671
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados