Cardiovascular disease in Noonan syndrome

Noonan syndrome

(2013) Amy E Roberts et al.   LANCET

Outcomes in children with Noonan syndrome and hypertrophic cardiomyopathy: A study from the Pediatric Cardiomyopathy Registry

(2012) James D. Wilkinson et al.   AMERICAN HEART JOURNAL

Atrioventricular canal defect in patients with RASopathies

(2012) Maria Cristina Digilio et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Survival Implications: Hypertrophic Cardiomyopathy in Noonan Syndrome

(2011) Edward J. Hickey et al.   Congenital Heart Disease

Molecular and clinical analysis ofRAF1in Noonan syndrome and related disorders: dephosphorylation of serine 259 as the essential mechanism for mutant activation

(2010) Tomoko Kobayashi et al.   HUMAN MUTATION

Noonan Syndrome: Clinical Features, Diagnosis, and Management Guidelines

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

PTPN11 Mutation Associated with Aortic Dilation and Hypertrophic Cardiomyopathy in a Pediatric Patient with Noonan Syndrome

(2009) John L. Jefferies et al.   PEDIATRIC CARDIOLOGY

Electrocardiography in Noonan syndromePTPN11 gene mutation—phenotype characterization

(2008) Ellen A. Croonen et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Clinical and molecular characterization of 40 patients with Noonan syndrome

(2008) Giovanni Battista Ferrero et al.   European Journal of Medical Genetics