Abstract
Congenital heart disease (CHD) is the most common congenital anomaly. Genetic causes are identified in 20-30% of CHD cases, particularly in non-isolated and familial forms. About a third of all CHD comprise of cardiac outflow tract (OFT) defects, including tetralogy of Fallot (TOF) and dextro-transposition of the great arteries (D-TGA). Using whole exome sequencing and genome-wide
| Original language | English |
|---|---|
| Qualification | Doctor of Philosophy |
| Awarding Institution |
|
| Supervisors/Advisors |
|
| Award date | 5 Feb 2025 |
| Print ISBNs | 9789464962932 |
| Publication status | Published - 2025 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
-
SDG 3 Good Health and Well-being
Fingerprint
Dive into the research topics of 'Rare and common variants in congenital heart disease: A complex puzzle to solve?'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver