Nephroblastomatosis or Wilms Tumor in a Fourth Patient With a Somatic PIK3CA Mutation
Wilms tumor and nephroblastomatosis are associated with syndromic conditions including hemihyperplasia. Hemihyperplasia is genetically heterogeneous and may be the result of genomic abnormalities seen in Beckwith-Wiedemann syndrome, mosaic chromosome or genomic abnormalities, or somatic point mutati...
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| Autores principales: | , , , , , , , , , , , , , |
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| Otros Autores: | |
| Lenguaje: | inglés |
| Publicado: |
Wiley
2019
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| Acceso en línea: | https://demo7.dspace.org/handle/123456789/473 |
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