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.