Current recommendations for clinical surveillance and genetic testing in rhabdoid tumor predisposition: a report from the SIOPE Host Genome Working Group

The rhabdoid tumor (RT) predisposition syndromes 1 and 2 (RTPS1 and 2) are rare genetic conditions rendering young children vulnerable to an increased risk of RT, malignant neoplasms affecting the kidney, miscellaneous soft-part tissues, the liver and the central nervous system (Atypical Teratoid Rh...

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Detalles Bibliográficos
Autores principales: Frühwald, M. C., Nemes, K., Boztug, H., Cornips, M. C. A., Evans, D. G., Farah, R., Glentis, S., Jorgensen, M., Katsibardi, K., Hirsch, S., Jahnukainen, K., Kventsel, I., Kerl, K., Kratz, C. P., Pajtler, K. W., Kordes, U., Ridola, V., Stutz, E., Bourdeaut, F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2021
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8484234/
https://www.ncbi.nlm.nih.gov/pubmed/33532948
http://dx.doi.org/10.1007/s10689-021-00229-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8484234/
https://www.ncbi.nlm.nih.gov/pubmed/33532948
http://dx.doi.org/10.1007/s10689-021-00229-1

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