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Noonan syndrome
Noonan syndrome is a genetic multisystem disorder characterised by distinctive facial features, developmental delay, learning difficulties, short stature, congenital heart disease, renal anomalies, lymphatic malformations, and bleeding difficulties. Mutations that cause Noonan syndrome alter genes e...
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| Publicado no: | Lancet |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4267483/ https://ncbi.nlm.nih.gov/pubmed/23312968 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/S0140-6736(12)61023-X |
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