Found: 4
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Association of Cx43 rs2071166 polymorphism with an increased risk for atrial septal defect.
- Published in:
- 2018
- By:
- Publication type:
- journal article
CpG site hypomethylation at ETS1-binding region regulates DLK1 expression in Chinese patients with Tetralogy of Fallot.
- Published in:
- Molecular Medicine Reports, 2022, v. 25, n. 3, p. N.PAG, doi. 10.3892/mmr.2022.12609
- By:
- Publication type:
- Article
Methylation status of CpG sites in the NOTCH4 promoter region regulates NOTCH4 expression in patients with tetralogy of Fallot.
- Published in:
- Molecular Medicine Reports, 2020, v. 22, n. 5, p. 4412
- By:
- Publication type:
- Article
A novel ZIC3 gene mutation identified in patients with heterotaxy and congenital heart disease.
- Published in:
- Scientific Reports, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41598-018-30204-3
- By:
- Publication type:
- Article