Hepatoblastoma in a child with a paternally-inherited ABCC8 mutation and mosaic paternal uniparental disomy 11p causing focal congenital hyperinsulinism
| Autor: | 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. |
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| Zdroj: | In European Journal of Medical Genetics February 2013 56(2):114-117 |
| Databáze: | ScienceDirect |
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