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Ellis-van Creveld Syndrome: Mutations Uncovered in Lebanese Families
Background. Ellis-van Creveld (EvC) syndrome is a rare, autosomal recessive disorder characterized by short stature, short limbs, growth retardation, polydactyly, and ectodermal defects with cardiac anomalies occurring in around 60% of cases. EVC syndrome has been linked to mutations in EVC and EVC2...
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| Autors principals: | , , , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Hindawi Limited
2015-01-01
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| Col·lecció: | Case Reports in Genetics |
| Accés en línia: | http://dx.doi.org/10.1155/2015/528481 |
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