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The Complex Genetic Basis of Congenital Heart Defects
Twenty years ago, chromosomal abnormalities were the only identifiable genetic causes of a small fraction of congenital heart defects (CHD). Today, a de novo or inherited genetic abnormality can be identified as pathogenic in one-third of cases. We refer to them here as monogenic causes, insofar as...
Sparad:
| I publikationen: | Circ J |
|---|---|
| Huvudupphovsmän: | , , , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
2017
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5715472/ https://ncbi.nlm.nih.gov/pubmed/28381817 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1253/circj.CJ-16-1343 |
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