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Pediatric Case of Li–Fraumeni Syndrome in Honduras
Li–Fraumeni syndrome is an inherited, autosomal dominant disease. It is categorized as a rare disease caused by mutations of the TP53 gene, which causes increased susceptibility of the patients and their children to many types of cancer. Choroid plexus tumor is rare, which occurs in 0.3 cases per 1,...
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| Publicado no: | Case Rep Pediatr |
|---|---|
| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Hindawi
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7814941/ https://ncbi.nlm.nih.gov/pubmed/33505750 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2021/6612802 |
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