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Noonan syndrome – a new survey
Noonan syndrome (NS) is an autosomal dominant disorder with vast heterogeneity in clinical and genetic features. Various symptoms have been reported for this abnormality such as short stature, unusual facial characteristics, congenital heart abnormalities, developmental complications, and an elevate...
Kaydedildi:
| Yayımlandı: | Arch Med Sci |
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| Asıl Yazarlar: | , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Termedia Publishing House
2016
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5206377/ https://ncbi.nlm.nih.gov/pubmed/28144274 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5114/aoms.2017.64720 |
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