Genetic basis of syndromes associated with congenital heart disease
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Cardiology and Cardiovascular Medicine
Reference72 articles.
1. Alagille syndrome.
2. Del(20p) with manifestations of arteriohepatic dysplasia
3. Localization of Alagille syndrome to 20p11.2-p12 by linkage analysis of a three-generation family
4. Mutations in the human Jagged1 gene are responsible for Alagille syndrome
5. Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1
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