Phenotypic variability in Hey2 ?/? mice and absence of HEY2 mutations in patients with congenital heart defects or Alagille syndrome
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics
Link
http://link.springer.com/content/pdf/10.1007/s00335-004-2389-x.pdf
Reference23 articles.
1. Syndromic paucity of interlobular bile ducts (Alagille syndrome or arteriohepatic dysplasia): Review of 80 cases
2. Tetralogy of Fallot and Other Congenital Heart Defects in Hey2 Mutant Mice
3. Evolution of Ventricular Septal Defect with Special Reference to Spontaneous Closure Rate, Subaortic Ridge and Aortic Valve Prolapse
4. Hey bHLH Factors in Cardiovascular Development
5. The Notch target genes Hey1 and Hey2 are required for embryonic vascular development
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