Calton, Elizabeth A <br/><br/>
Hepatoblastoma in a child with a paternally-inherited ABCC8 mutation and mosaic paternal uniparental disomy 11p causing focal congenital hyperinsulinism.  [electronic resource] 

 -  European journal of medical genetics  Feb 2013 
 - 114-7 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1878-0849 
<br/><br/><label>Standard No.: </label>10.1016/j.ejmg.2012.12.001  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>ATP-Binding Cassette Transporters--genetics<br/>Chromosomes, Human, Pair 11<br/>Congenital Hyperinsulinism--complications<br/>Hepatoblastoma--diagnosis<br/>Humans<br/>Infant<br/>Liver Neoplasms--diagnosis<br/>Male<br/>Microsatellite Repeats<br/>Mosaicism<br/>Mutation<br/>Positron-Emission Tomography<br/>Potassium Channels, Inwardly Rectifying--genetics<br/>Receptors, Drug--genetics<br/>Sulfonylurea Receptors<br/>Tomography, X-Ray Computed<br/>Uniparental Disomy