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Familial Dermal Eccrine Cylindromatosis with Emphasis on Histology and Genetic Mapping
Familial cylindromatosis (FC) is an autosomal dominant disorder with apparently complete penetrance, but variable expression. There is an increasing evidence that FC is clinically, genetically, and histologically heterogeneous disorder as the simultaneous occurrence of cylindromas and other tumors o...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Medknow Publications & Media Pvt Ltd
2013
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3853602/ https://www.ncbi.nlm.nih.gov/pubmed/24349843 http://dx.doi.org/10.4103/2141-9248.121207 |