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Diagnostic Test for Alagille Syndrome
Identifies Jagged 1 mutations and intragenic alterations Market NeedAlagille syndrome (AGS) is a highly variable, multi-system, autosomal dominant disorder that affects at least 1 in 70,000 newborns. It is often associated with neonatal jaundice and has traditionally been diagnosed based on bile duct paucity and resultant liver disease, in combinat...
Published: 5/9/2017   |   Inventor(s): Nancy Spinner, Ian Krantz
Keywords(s): Alagille Syndrome (AGS)
Category(s): Diagnostic