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Congenital heart defects in Noonan syndrome: Diagnosis, management, and treatment
Noonan syndrome is a pleomorphic genetic disorder, in which a high percentage of affected individuals have cardiovascular involvement, most prevalently various forms of congenital heart disease (i.e., pulmonary valve stenosis, septal defects, left-sided lesions, and complex forms with multiple anoma...
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| Publicado en: | Am J Med Genet C Semin Med Genet |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
2020
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7682536/ https://ncbi.nlm.nih.gov/pubmed/32022400 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.c.31765 |
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