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Article

Genetic analysis of the TBX20 gene promoter region in patients with ventricular septal defects

22 Mar 2012

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 22465533
DOI: 10.1016/j.gene.2012.03.055

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Related research

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Click a neighbor to travelStep 1 · 12 closest

Genetic analysis of the TBX20 gene promoter region in patients with ventricular septal defectsPMID 22465533Read ↗

Novel and functional sequence variants within the TBX2 gene promoter in ventricular septal defects.Semantic proximity Read ↗

Genetic analysis of the TBX1 gene promoter in ventricular septal defects.Semantic proximity Read ↗

Familial cardiac septal defect due to a novel nine-base deletion in TBX20.Semantic proximity Read ↗

Novel and functional variants within the TBX18 gene promoter in ventricular septal defects.Semantic proximity Read ↗

[Association between the SNPs of human Tbx20 gene and congenital atrial septal defects in Uygur population of Xinjiang region].Semantic proximity Read ↗

Genetic analysis of the TBX3 gene promoter in ventricular septal defects.Semantic proximity Read ↗

Identification of a novel and functional mutation in the TBX5 gene in a patient by screening from 354 patients with isolated ventricular septal defectSemantic proximity Read ↗

Mild decrease in TBX20 promoter activity is a potentially protective factor against congenital heart defects in the Han Chinese population.Semantic proximity Read ↗

TBX20 loss-of-function mutation contributes to double outlet right ventricle.Semantic proximity Read ↗

TBX20 loss-of-function mutation responsible for familial tetralogy of Fallot or sporadic persistent truncus arteriosus.Semantic proximity Read ↗

A novel TBX20 loss‑of‑function mutation contributes to adult‑onset dilated cardiomyopathy or congenital atrial septal defect.Semantic proximity Read ↗

Copy number variation analysis in bicuspid aortic valve-related aortopathy identifies TBX20 as a contributing geneSemantic proximity Read ↗

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