- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
2056-9920
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Retinoblastoma and mosaic 13q deletion: a case report ; volume:7 ; number:1 ; day:3 ; month:9 ; year:2021 ; pages:1-6 ; date:12.2021
International Journal of Retina and Vitreous ; 7, Heft 1 (3.9.2021), 1-6, 12.2021
- Creator
-
Gargallo, Pablo
Oltra, Silvestre
Balaguer, Julia
Barranco, Honorio
Yáñez, Yania
Segura, Vanessa
Juan-Ribelles, Antonio
Calabria, Inés
Llavador, Margarita
Castel, Victoria
Cañete, Adela
- Contributor
-
SpringerLink (Online service)
- DOI
-
10.1186/s40942-021-00321-9
- URN
-
urn:nbn:de:101:1-2021111620512285378447
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:35 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Gargallo, Pablo
- Oltra, Silvestre
- Balaguer, Julia
- Barranco, Honorio
- Yáñez, Yania
- Segura, Vanessa
- Juan-Ribelles, Antonio
- Calabria, Inés
- Llavador, Margarita
- Castel, Victoria
- Cañete, Adela
- SpringerLink (Online service)
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Retinoblastoma
Cytomegalovirus Retinitis in an Eye with Unilateral Retinoblastoma: A Case Report
13q mosaic deletion including RB1 associated to mild phenotype and no cancer outcome – case report and review of the literature
Prader-Willi syndrome patient with atypical phenotypes caused by mosaic deletion in the paternal 15q11-q13 region: a case report
Surgical resection of retinoblastoma-associated bladder leiomyosarcoma during pregnancy: a case report
When the second comes first– rhabdomyosarcoma preceding heritable retinoblastoma– a case report
Metastatic retinoblastoma of the parotid and submandibular glands: a rare case report
Unilateral retinoblastoma, autism spectrum disorder and macrocrania in 13q deletion syndrome: a case report
Digital Gangrene and Antiphospholipid Syndrome in a Retinoblastoma Patient with Chromosome 13q Deletion: A Case Report
Diffuse Anterior Retinoblastoma Masquerading as Complicated Cataract-A Case Report
Familial deletion 18p syndrome: case report
Cryptic FMR1 mosaic deletion in a phenotypically normal mother of a boy with fragile X syndrome: case report
Retinoblastoma
Cytomegalovirus Retinitis in an Eye with Unilateral Retinoblastoma: A Case Report
13q mosaic deletion including RB1 associated to mild phenotype and no cancer outcome – case report and review of the literature
Prader-Willi syndrome patient with atypical phenotypes caused by mosaic deletion in the paternal 15q11-q13 region: a case report
Surgical resection of retinoblastoma-associated bladder leiomyosarcoma during pregnancy: a case report
When the second comes first– rhabdomyosarcoma preceding heritable retinoblastoma– a case report