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Clinical manifestations of Noonan syndrome
Noonan syndrome is a common genetic disorder characterized by facial anomalies, congenital heart defect, short stature, webbed neck, chest deformities and undescended testes. The phenotypic expression of Noonan syndrome is extremely variable, with some affected subjects showing only minor features o...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2001
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3232501/ https://www.ncbi.nlm.nih.gov/pubmed/22368597 |