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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...
| Autores principales: | , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Elsevier
2020
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7666322/ https://www.ncbi.nlm.nih.gov/pubmed/33224486 http://dx.doi.org/10.1016/j.amsu.2020.10.063 |