Wordt geladen...
Ellis–Van Creveld syndrome in siblings: A rare case report
Ellis–Van Creveld syndrome or chondroectodermal dysplasia is a rare autosomal recessive disorder presenting several skeletal manifestations and congenital heart malformations. Ellis–Van Creveld syndrome comprises of a tetrad of clinical manifestations of chondrodysplasia, polydactyly, ectodermal dys...
Bewaard in:
| Gepubliceerd in: | J Pharm Bioallied Sci |
|---|---|
| Hoofdauteurs: | , , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Medknow Publications & Media Pvt Ltd
2016
|
| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5074027/ https://ncbi.nlm.nih.gov/pubmed/27829775 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0975-7406.191954 |
| Tags: |
Voeg label toe
Geen labels, Wees de eerste die dit record labelt!
|