Congenital heart defects in Noonan syndrome and RIT1 mutation
- 1 December 2016
- journal article
- Published by Elsevier BV in Genetics in Medicine
- Vol. 18 (12), 1320
- https://doi.org/10.1038/gim.2016.137
Abstract
No abstract availableKeywords
This publication has 3 references indexed in Scilit:
- Genotype and phenotype in patients with Noonan syndrome and a RIT1 mutationGenetics in Medicine, 2016
- Atrioventricular canal defect in patients with RASopathiesEuropean Journal of Human Genetics, 2012
- Epidemiology and Cause-Specific Outcome of Hypertrophic Cardiomyopathy in ChildrenCirculation, 2007