Germline GPR161 Mutations Predispose to Pediatric Medulloblastoma

PURPOSE: The identification of a heritable tumor predisposition often leads to changes in management and increased surveillance of individuals who are at risk; however, for many rare entities, our knowledge of heritable predisposition is incomplete. METHODS: Families with childhood medulloblastoma,...

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Detalles Bibliográficos
Autores principales: Begemann, Matthias, Waszak, Sebastian M., Robinson, Giles W., Jäger, Natalie, Sharma, Tanvi, Knopp, Cordula, Kraft, Florian, Moser, Olga, Mynarek, Martin, Guerrini-Rousseau, Lea, Brugieres, Laurence, Varlet, Pascale, Pietsch, Torsten, Bowers, Daniel C., Chintagumpala, Murali, Sahm, Felix, Korbel, Jan O., Rutkowski, Stefan, Eggermann, Thomas, Gajjar, Amar, Northcott, Paul, Elbracht, Miriam, Pfister, Stefan M., Kontny, Udo, Kurth, Ingo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Clinical Oncology 2020
Materias:
ORIGINAL REPORTS
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6943973/
https://www.ncbi.nlm.nih.gov/pubmed/31609649
http://dx.doi.org/10.1200/JCO.19.00577

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6943973/
https://www.ncbi.nlm.nih.gov/pubmed/31609649
http://dx.doi.org/10.1200/JCO.19.00577

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