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Replication of the 4p16 Susceptibility Locus in Congenital Heart Disease in Han Chinese Populations
Congenital heart disease (CHD) is the most common form of congenital human birth anomalies and a leading cause of perinatal and infant mortality. Some studies including our published genome-wide association study (GWAS) of CHD have indicated that genetic variants may contribute to the risk of CHD. R...
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| Autors principals: | , , , , , , , , , , , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Public Library of Science
2014
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4162603/ https://ncbi.nlm.nih.gov/pubmed/25215500 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0107411 |
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