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13q interstitial deletion in a moroccan child with hereditary retinoblastoma and intellectual disability: A case report
Retinoblastoma is the most common malignant tumor of the eye in children (incidence:1/15,000 to 1/20,000 births), with a sex ratio of 1,5/1. Retinoblastoma, in its inherited form, is a disease caused by a syndrome of genetic predisposition to cancer. The RB1 gene, a tumor suppressor gene, is localiz...
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| Publicat a: | Ann Med Surg (Lond) |
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| Autors principals: | , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Elsevier
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7666322/ https://ncbi.nlm.nih.gov/pubmed/33224486 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.amsu.2020.10.063 |
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