A carregar...
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,...
Na minha lista:
| Publicado no: | North Clin Istanb |
|---|---|
| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Kare Publishing
2015
|
| Assuntos: | |
| Acesso em linha: | 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 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|