Condition: Septal hypertrophy
rs121918455 in
PTPN11 gene and
Septal hypertrophy
PMID 19077116 2009 Genotype differences in cognitive functioning in Noonan syndrome.
PMID 11992261 2002 PTPN11 mutations in Noonan syndrome: molecular spectrum, genotype-phenotype correlation, and phenotypic heterogeneity.
PMID 12960218 2003 Correlation between PTPN11 gene mutations and congenital heart defects in Noonan and LEOPARD syndromes.
PMID 16124853 2005 Noonan syndrome and related disorders: genetics and pathogenesis.