Alagille syndrome
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology and Child Health
Link
http://link.springer.com/content/pdf/10.1007/BF02723697.pdf
Reference28 articles.
1. Alagille D, Estrada A, Hadchouel Met al. Syndrome paucity of interlobular bile ducts (Alagille syndrome or arteriohepatic dysplasia): Review of 80 cases.J Pediatr 1987; 110:195–200.
2. Li L, Krantz ID, Deng Yet al. Alagille syndrome is caused by mutations in human jaggedl, which encodes a ligand for Notch.Nat Genet 1997; 16:243–251.
3. Oda T, Elkahloun AG, Pike BL, Okajima Ket al. Mutations in the human Jaggedl gene are responsible for Alagille syndrome.Nat Genet 1997; 16:235–242.
4. Spinner NB, Colliton RP, Crosnier C, Krantz ID, Hadchouel M, Meunier-Rotival M: Jaggedl mutations in Alagille syndrome.Hum Mutat 2001; 17:18–33.
5. Emerick KM, Rand EB, Goldmuntz Eet al. Features of Alagille syndrome in 92 patients: frequency and relation to prognosis.Hepatology 1999; 29:822–829.
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