Genetics Research

ISSN : 0016-6723
1 publication(s) trouvée(s)
Article scientifique
A severe clinical phenotype of Noonan syndrome with neonatal hypertrophic cardiomyopathy in the second case worldwide withRAF1S259Y neomutation
Noonan syndrome and related disorders are a group of clinically and genetically heterogeneous conditions caused by mutations in genes of …
2019 Open Access