Wordt geladen...
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...
Bewaard in:
| Gepubliceerd in: | Arch Med Sci |
|---|---|
| Hoofdauteurs: | , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Termedia Publishing House
2016
|
| Onderwerpen: | |
| Online toegang: | 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 |
| Tags: |
Voeg label toe
Geen labels, Wees de eerste die dit record labelt!
|