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Molecular Genetics and Complex Inheritance of Congenital Heart Disease
Congenital heart disease (CHD) is the most common congenital malformation and the leading cause of mortality therein. Genetic etiologies contribute to an estimated 90% of CHD cases, but so far, a molecular diagnosis remains unsolved in up to 55% of patients. Copy number variations and aneuploidy acc...
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| Publicat a: | Genes (Basel) |
|---|---|
| Autors principals: | , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
MDPI
2021
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8307500/ https://ncbi.nlm.nih.gov/pubmed/34209044 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/genes12071020 |
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