Phenotypic analysis of individuals with Costello syndrome due to HRAS p.G13C

High incidence of progressive postnatal cerebellar enlargement in Costello syndrome: Brain overgrowth associated withHRASmutations as the likely cause of structural brain and spinal cord abnormalities

(2010) Karen W. Gripp et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Longitudinal course of cognitive, adaptive, and behavioral characteristics in Costello syndrome

(2009) Marni E. Axelrad et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Elements of morphology: Standard terminology for the periorbital region

(2009) Bryan D. Hall et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

A premature infant with Costello syndrome due to a rare G13CHRASmutation

(2009) Maria Piccione et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Practical Guidelines for Evaluation of Loose Anagen Hair Syndrome

(2009) Julie L. Cantatore-Francis et al.   ARCHIVES OF DERMATOLOGY

Activating mutations in FGFR3 and HRAS reveal a shared genetic origin for congenital disorders and testicular tumors

(2009) Anne Goriely et al.   NATURE GENETICS

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

(2009) Viviana Cordeddu et al.   NATURE GENETICS

Prenatal features of Costello syndrome: ultrasonographic findings and atrial tachycardia

(2009) Angela E. Lin et al.   PRENATAL DIAGNOSIS

Costello syndrome associated with novel germlineHRAS mutations: An attenuated phenotype?

(2008) Karen W. Gripp et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

OncogenicHRASmutations cause prolonged PI3K signaling in response to epidermal growth factor in fibroblasts of patients with Costello syndrome

(2008) Georg Rosenberger et al.   HUMAN MUTATION