Retinoblastoma and mosaic 13q deletion: a case report

BACKGROUND: Patients with 13q-syndrome are at risk of retinoblastoma when the RB1 gene, located in the chromosomal band 13q14.2, is deleted. This syndrome is frequently associated with congenital malformations and developmental delay, although these signs could be mild. Mosaic 13q-deletion patients...

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Detalles Bibliográficos
Autores principales: Gargallo, Pablo, Oltra, Silvestre, Balaguer, Julia, Barranco, Honorio, Yáñez, Yania, Segura, Vanessa, Juan-Ribelles, Antonio, Calabria, Inés, Llavador, Margarita, Castel, Victoria, Cañete, Adela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8418035/
https://www.ncbi.nlm.nih.gov/pubmed/34479642
http://dx.doi.org/10.1186/s40942-021-00321-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8418035/
https://www.ncbi.nlm.nih.gov/pubmed/34479642
http://dx.doi.org/10.1186/s40942-021-00321-9

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