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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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| Pubblicato in: | Lancet |
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| Autori principali: | , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
2013
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| Soggetti: | |
| Accesso online: | 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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