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

Gustavo Dib DangoniAnne Caroline Barbosa TeixeiraTalita Ferreira AguiarSofia Mizuho Miura SugayamaVicente Odone FilhoDébora Romeo BertolaAna Cristina Victorino Krepischi
Published in: Pediatric blood & cancer (2023)
Keyphrases
  • rare case
  • intellectual disability
  • mental health
  • dna repair