Identification and Cloning of the Human Homolog (JAG1) of the RatJagged1Gene from the Alagille Syndrome Critical Region at 20p12
Open Access
- 1 August 1997
- Vol. 43 (3) , 376-379
- https://doi.org/10.1006/geno.1997.4820
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- Localization of Alagille syndrome to 20p11.2-p12 by linkage analysis of a three-generation familyHuman Genetics, 1995
- Jagged: A mammalian ligand that activates notch1Cell, 1995
- Deleted Chromosome 20 from a patient with Alagille syndrome isolated in a cell hybrid through leucine transport selection: study of three candidate genesMammalian Genome, 1994
- Segregation analysis of Alagille syndrome.Journal of Medical Genetics, 1994
- Alagille syndrome and deletion of 20p.Journal of Medical Genetics, 1990
- Basic local alignment search toolJournal of Molecular Biology, 1990
- Construction and characterization of a yeast artificial chromosome library containing seven haploid human genome equivalents.Proceedings of the National Academy of Sciences, 1990
- Syndromic paucity of interlobular bile ducts (Alagille syndrome or arteriohepatic dysplasia): Review of 80 casesThe Journal of Pediatrics, 1987
- Del(20p) with manifestations of arteriohepatic dysplasiaAmerican Journal of Medical Genetics, 1986
- Hepatic ductular hypoplasia associated with characteristic facies, vertebral malformations, retarded physical, mental, and sexual development, and cardiac murmurThe Journal of Pediatrics, 1975