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A rare case of hepatoblastoma in a syndromic child with a de novo germline JAG1 mutation.

Pediatric blood & cancer - 1 Jul 2023

Dangoni Gustavo Dib, Teixeira Anne Caroline Barbosa, Aguiar Talita Ferreira, Sugayama Sofia Mizuho Miura, Filho Vicente Odone, Bertola Débora Romeo, Krepischi Ana Cristina Victorino

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Share to Abnormalities, Multiple
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Share to Genetic Diseases, X-Linked

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Hepatoblastoma

Share to Ichthyosiform Erythroderma, Congenital

Share to Jagged-1 Protein

Share to Limb Deformities, Congenital

Share to Liver Neoplasms

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Identifiers

PMID: 36965188
DOI: 10.1002/pbc.30311

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

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