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Variants in GATA4 Are a Rare Cause of Familial and Sporadic Congenital Diaphragmatic Hernia
Congenital diaphragmatic hernia (CDH) is characterized by incomplete formation of the diaphragm, occurring as either an isolated defect or in association with other anomalies. Genetic factors including aneuploidies and copy number variants are important in the pathogenesis of many cases of CDH, but...
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| Autors principals: | , , , , , , , , , , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2012
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3570587/ https://ncbi.nlm.nih.gov/pubmed/23138528 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00439-012-1249-0 |
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