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Recurrent Sporadic Bilateral Retinoblastoma in a Child with 13q Deletion Syndrome
13q syndrome is a chromosomal abnormality in which there is a pathognomic deletion of the genetic material on the long arm (q) of chromosome 13. Phenotypes of this syndrome are variable depending on the location of the deleted segment. The main manifestations of the syndrome include mental retardati...
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Cureus
2020
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7008771/ https://www.ncbi.nlm.nih.gov/pubmed/32064198 http://dx.doi.org/10.7759/cureus.6618 |