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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...
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| Publicado no: | J Pharm Bioallied Sci |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Medknow Publications & Media Pvt Ltd
2016
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| Assuntos: | |
| Acesso em linha: | 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 |
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