Hepatoblastoma in a child with a paternally-inherited ABCC8 mutation and mosaic paternal uniparental disomy 11p causing focal congenital hyperinsulinism. [electronic resource]
Producer: 20130715Description: 114-7 p. digitalISSN:- 1878-0849
- ATP-Binding Cassette Transporters -- genetics
- Chromosomes, Human, Pair 11
- Congenital Hyperinsulinism -- complications
- Hepatoblastoma -- diagnosis
- Humans
- Infant
- Liver Neoplasms -- diagnosis
- Male
- Microsatellite Repeats
- Mosaicism
- Mutation
- Positron-Emission Tomography
- Potassium Channels, Inwardly Rectifying -- genetics
- Receptors, Drug -- genetics
- Sulfonylurea Receptors
- Tomography, X-Ray Computed
- Uniparental Disomy
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Publication Type: Case Reports; Journal Article
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