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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Autori principali: Gripp, Karen W, Baker, Laura, Kandula, Vinay, Conard, Katrina, Scavina, Mena, Napoli, Joseph A, Griffin, Gregory C, Thacker, Mihir, Knox, Rachel G, Clark, Graeme, Parker, Victoria ER, Semple, Robert, Mirzaa, Ghayda, Keppler-Noreuil, Kim M
Altri autori: Integrated Molecular Plant physiology Research (IMPRES)
Lingua:inglese
Pubblicazione: Wiley 2019
Accesso online:https://demo7.dspace.org/handle/123456789/473
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