Abstrait
Le néphroblastome, ou tumeur de Wilms, et le neuroblastome sont, comme le rétinoblastome, des tumeurs embryonnaires atteignant le jeune enfant. Il a été tentant d’extrapoler la théorie mutationnelle proposée pour la rétinoblastome à ces deux types de tumeurs (1, 2), mais nous verrons que les choses ne sont pas aussi simples.
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Bonaïti-Pellié, C. (2009). Cas familiaux de néphroblastomes et de neuroblastomes. In: Épidémiologie des cancers de l’enfant. Springer, Paris. https://doi.org/10.1007/978-2-287-78337-1_35
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DOI: https://doi.org/10.1007/978-2-287-78337-1_35
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