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A rare case report of Ellis Van Creveld syndrome in an Indian patient and literature review
Ellis Van Creveld syndrome (EVC) is a rare genetic disorder having autosomal recessive inheritance affecting the Amish population of Pennsylvania in USA with incidence of 1:244,000 for the general population. This syndrome consists of characteristic features such as bilateral postaxial polydactyly,...
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Publicado no: | J Oral Biol Craniofac Res |
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Main Authors: | , , , |
Formato: | Artigo |
Idioma: | Inglês |
Publicado em: |
Elsevier
2015
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Assuntos: | |
Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4523583/ https://ncbi.nlm.nih.gov/pubmed/26258022 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jobcr.2015.05.003 |
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