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Hepatoblastoma in a child with a paternally-inherited ABCC8 mutation and mosaic paternal uniparental disomy 11p causing focal congenital hyperinsulinism
✍ Scribed by Calton, Elizabeth A.; Temple, I. Karen; Mackay, Deborah J.G.; Lever, Margaret; Ellard, Sian; Flanagan, Sarah E.; Davies, Justin H.; Hussain, Khalid; Gray, Juliet C.
- Book ID
- 120393160
- Publisher
- Elsevier Science
- Year
- 2013
- Tongue
- English
- Weight
- 169 KB
- Volume
- 56
- Category
- Article
- ISSN
- 1769-7212
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