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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...
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| Опубликовано в: : | Arch Med Sci |
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| Главные авторы: | , , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
Termedia Publishing House
2016
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| Предметы: | |
| Online-ссылка: | 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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