Clinical utility gene card for: Alagille Syndrome (ALGS)

NOTCH2 Mutations Cause Alagille Syndrome, a Heterogeneous Disorder of the Notch Signaling Pathway

Ryan M. McDaniell, Daniel M. Warthen, Pedro A. Sanchez‐Lara et al. · The American Journal of Human Genetics · 2006 · 743 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

Syndromic paucity of interlobular bile ducts (Alagille syndrome or arteriohepatic dysplasia): Review of 80 cases

D Alagille, Andrea Estrada, Michelle Hadchouel et al. · The Journal of Pediatrics · 1987 · 669 citations

Medicine, Internal Medicine, Pathology +14

Features of Alagille Syndrome in 92 Patients: Frequency and Relation to Prognosis

Karan M. Emerick, Elizabeth B. Rand, Elizabeth Goldmuntz et al. · Hepatology · 1999 · 664 citations · Full text

Medicine, Pathology, Pediatrics +17

Analysis of Cardiovascular Phenotype and Genotype-Phenotype Correlation in Individuals With a <i>JAG1</i> Mutation and/or Alagille Syndrome

Doff B. McElhinney, Ian D. Krantz, Lynn Bason et al. · Circulation · 2002 · 308 citations

Medicine, Cardiology, Genetics +16

Arteriohepatic dysplasia: Familial pulmonary arterial stenosis with neonatal liver disease

G. H. Watson, Vincent T. Miller · Archives of Disease in Childhood · 1973 · 266 citations · Full text

Medicine, Genetics, Pediatrics +17