Condition: NOONAN SYNDROME 7
rs121913369 in
BRAF gene and
NOONAN SYNDROME 7
PMID 19206169 2009 Germline BRAF mutations in Noonan, LEOPARD, and cardiofaciocutaneous syndromes: molecular diversity and associated phenotypic spectrum.
PMID 20876176 2010 Noonan syndrome: clinical features, diagnosis, and management guidelines.