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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Detalles Bibliográficos
Autores principales: Outtaleb, F.Z., Kora, L., Jabrane, G., Serbati, N., El Maaloum, L., Allali, B., El Kettani, A., Dehbi, H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Case Report
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

Internet

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

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