Coarctation of the aorta in Noonan-like syndrome with loose anagen hair

Noonan syndrome due to aSHOC2mutation presenting with fetal distress and fatal hypertrophic cardiomyopathy in a premature infant

(2012) Rebecca Hoban et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Clinical and molecular analysis of RASopathies in a group of Turkish patients

(2012) PÖ Şimşek-Kiper et al.   CLINICAL GENETICS

Co-occurring SHOC2 and PTPN11 mutations in a patient with severe/complex Noonan syndrome-like phenotype

(2011) Sara Ekvall et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Spectrum of Mutations in Noonan Syndrome and Their Correlation with Phenotypes

(2011) Beom Hee Lee et al.   JOURNAL OF PEDIATRICS

Mutation analysis of the SHOC2 gene in Noonan-like syndrome and in hematologic malignancies

(2010) Shoko Komatsuzaki et al.   JOURNAL OF HUMAN GENETICS

Noonan Syndrome: Clinical Features, Diagnosis, and Management Guidelines

(2010) A. A. Romano et al.   PEDIATRICS

Mutation of SHOC2 promotes aberrant protein N-myristoylation and causes Noonan-like syndrome with loose anagen hair

(2009) Viviana Cordeddu et al.   NATURE GENETICS