Found: 9
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A Novel NKX2.6 Mutation Associated with Congenital Ventricular Septal Defect.
- Published in:
- Pediatric Cardiology, 2015, v. 36, n. 3, p. 646, doi. 10.1007/s00246-014-1060-x
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- Article
Meta-analysis of clinical studies comparing coronary artery bypass grafting with percutaneous coronary intervention in patients with end-stage renal disease.
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- European Journal of Cardio-Thoracic Surgery, 2013, v. 43, n. 3, p. 459, doi. 10.1093/ejcts/ezs360
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- Article
Identification of SOX18 as a New Gene Predisposing to Congenital Heart Disease.
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- Diagnostics (2075-4418), 2022, v. 12, n. 8, p. 1917, doi. 10.3390/diagnostics12081917
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- Article
NR2F2 loss-of-function mutation is responsible for congenital bicuspid aortic valve.
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- International Journal of Molecular Medicine, 2019, v. 43, n. 4, p. 1839
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- Article
Discovery of GJC1 (Cx45) as a New Gene Underlying Congenital Heart Disease and Arrhythmias.
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- Biology (2079-7737), 2023, v. 12, n. 3, p. 346, doi. 10.3390/biology12030346
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- Article
GATA4 Loss-of-Function Mutations Underlie Familial Tetralogy of Fallot.
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- Human Mutation, 2013, v. 34, n. 12, p. 1662, doi. 10.1002/humu.22434
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- Article
Somatic GATA4 mutation contributes to tetralogy of Fallot.
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- Experimental & Therapeutic Medicine, 2024, v. 27, n. 2, p. N.PAG, doi. 10.3892/etm.2024.12379
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- Article
TBX1 loss-of-function mutation contributes to congenital conotruncal defects.
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- Experimental & Therapeutic Medicine, 2018, v. 15, n. 1, p. 447, doi. 10.3892/etm.2017.5362
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- Article
SMAD1 Loss-of-Function Variant Responsible for Congenital Heart Disease.
- Published in:
- BioMed Research International, 2022, p. 1, doi. 10.1155/2022/9916325
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- Article