Noonan syndrome

Impaired Sertoli Cell Function in Males Diagnosed with Noonan Syndrome

(2011) K.A. Marcus et al.   JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM

PTPN11analysis for the prenatal diagnosis of Noonan syndrome in fetuses with abnormal ultrasound findings

(2009) KA Lee et al.   CLINICAL GENETICS

The RASopathies: developmental syndromes of Ras/MAPK pathway dysregulation

(2009) William E Tidyman et al.   CURRENT OPINION IN GENETICS & DEVELOPMENT

Growth Hormone and the Heart in Noonan Syndrome

(2009) C. Noordam   HORMONE RESEARCH

Noonan Syndrome, the Ras–MAPK Signalling Pathway and Short Stature

(2009) Gerhard Binder   Hormone Research in Paediatrics

Noonan Syndrome and Related Disorders: A Review of Clinical Features and Mutations in Genes of the RAS/MAPK Pathway

(2009) Alexander A.L. Jorge et al.   Hormone Research in Paediatrics

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

(2009) Viviana Cordeddu et al.   NATURE GENETICS

A restricted spectrum of NRAS mutations causes Noonan syndrome

(2009) Ion C Cirstea et al.   NATURE GENETICS

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