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Case Report - Alagille syndrome with prominent skin manifestations, 12/2005
Alagille syndrome, a rare genetic disorder with autosomal dominant transmission, manifests 5 major features: paucity of interlobular bile ducts, characteristic... 
Alagille syndrome, Arteriohepatic dysplasia, Xanthomata
Journal
Journal of Pediatric Gastroenterology and Nutrition, ISSN 0277-2116, 03/2018, Volume 67, Issue 2, pp. 148 - 156
Journal Article
Obstetric Medicine, ISSN 1753-495X, 2019, p. 1753495
Journal Article
Journal Article
Journal of Pediatric Gastroenterology and Nutrition, ISSN 0277-2116, 01/2017, Volume 64, Issue 6, pp. 888 - 891
Journal Article
Paediatrics and Child Health, ISSN 1751-7222, 12/2018, Volume 28, Issue 12, pp. 574 - 578
Congenital heart disease affects around 0.7% of liveborn infants and is the most frequent cause of death from congenital malformations. This review will... 
marfan syndrome | noonan syndrome | Alagille syndrome | trisomy 21 | Down syndrome | 22q11 deletion | Turner syndrome | Holt-Oram syndrome | Williams syndrome | Loeys-Dietz syndrome | CHARGE syndrome | congenital heart disease | Kabuki syndrome | Genetic disorders | Research | Comorbidity | Heart diseases | Analysis | Patient outcomes
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 2006, Volume 79, Issue 1, pp. 169 - 173
Journal Article
Journal Article
Journal of pediatric surgery, ISSN 0022-3468, 05/2019
Alagille syndrome (ALGS) is an autosomal dominant disorder, characterized by a paucity of intrahepatic bile ducts, resulting in significant cholestasis, and... 
Journal Article
Pediatric and Developmental Pathology, ISSN 1093-5266, 1/2018, Volume 21, Issue 1, pp. 79 - 83
Alagille syndrome is a multisystem disorder classically involving the liver, heart, vertebrae, facial features, and the eyes. In this case report, we document... 
jaundice | JAG1 | Alagille syndrome | cholestasis | CK7 | JAG1 MUTATIONS | DIAGNOSIS | CHOLEDOCHAL CYSTS | PAUCITY | PEDIATRICS | PATHOLOGY | FEATURES | Alagille Syndrome - genetics | Alagille Syndrome - diagnosis | Humans | Alagille Syndrome - complications | Male | Alagille Syndrome - pathology | Genetic Markers | Mutation, Missense | Infant, Newborn | Jagged-1 Protein - genetics | Index Medicus
Journal Article
ANNALES DE BIOLOGIE CLINIQUE, ISSN 0003-3898, 11/2018, Volume 76, Issue 6, pp. 675 - 680
We report the case of an infant hospitalized for neonatal anoxic isehemia in whom the diagnosis of Alagille syndrome (SAG ; MIM # 118450) was suspected in the... 
MEDICINE, RESEARCH & EXPERIMENTAL | DIAGNOSIS | Alagille syndrome | JAGGED1 | JAG1 gene | bisalbuminemia | MEDICAL LABORATORY TECHNOLOGY
Journal Article