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General approach to velocardiofacial anomalies: a pediatric case presenting with Fallot tetralogy
Velocardiofacial syndrome (VCFS), also known as “Shprintzen syndrome” or “22q11.2 deletion syndrome” is an autosomal dominant genetic disorder with a wide range of phenotypical findings. It is majorly characterized by cleft palate, dysmorphic face, conotruncal cardiac anomalies, growth retardation,...
Gorde:
| Argitaratua izan da: | North Clin Istanb |
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| Egile Nagusiak: | , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
Kare Publishing
2015
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5175041/ https://ncbi.nlm.nih.gov/pubmed/28058329 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.14744/nci.2014.04695 |
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