A review of craniofacial and dental findings of the RASopathies

RASA1somatic mutation and variable expressivity in capillary malformation/arteriovenous malformation (CM/AVM) syndrome

(2016) Colleen F. Macmurdo et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Pathogenetics of the RASopathies

(2016) William E. Tidyman et al.   HUMAN MOLECULAR GENETICS

Café-au-lait Macules and Neurofibromatosis Type 1: A Review of the Literature

(2016) Anne Bernier et al.   PEDIATRIC NEUROLOGY

Recent advances in RASopathies

(2015) Yoko Aoki et al.   JOURNAL OF HUMAN GENETICS

Craniofacial and dental development in Costello syndrome

(2014) Alice F. Goodwin et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

LEOPARD Syndrome

(2014) Ikenna Valentine Aboh et al.   JOURNAL OF CRANIOFACIAL SURGERY

Cardio-Facio-Cutaneous Syndrome: Clinical Features, Diagnosis, and Management Guidelines

(2014) M. E. M. Pierpont et al.   PEDIATRICS

Gain-of-Function Mutations in RIT1 Cause Noonan Syndrome, a RAS/MAPK Pathway Syndrome

(2013) Yoko Aoki et al.   AMERICAN JOURNAL OF HUMAN GENETICS

The RASopathies

(2013) Katherine A. Rauen   Annual Review of Genomics and Human Genetics

Abnormal Ras signaling in Costello syndrome (CS) negatively regulates enamel formation

(2013) Alice F. Goodwin et al.   HUMAN MOLECULAR GENETICS

Case report: Noonan syndrome with multiple giant cell lesions and review of the literature

(2012) Julia Karbach et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Craniofacial and dental development in cardio-facio-cutaneous syndrome: the importance of Ras signaling homeostasis

(2012) AF Goodwin et al.   CLINICAL GENETICS

Review and update ofSPRED1mutations causing legius syndrome

(2012) Hilde Brems et al.   HUMAN MUTATION

Noonan syndrome and clinically related disorders

(2011) Marco Tartaglia et al.   BEST PRACTICE & RESEARCH CLINICAL ENDOCRINOLOGY & METABOLISM

Noonan Syndrome: Clinical Features, Diagnosis, and Management Guidelines

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

Genetic and Pathogenetic Aspects of Noonan Syndrome and Related Disorders

(2009) Martin Zenker   HORMONE RESEARCH

The RAS/MAPK syndromes: novel roles of the RAS pathway in human genetic disorders

(2008) Yoko Aoki et al.   HUMAN MUTATION

Leopard syndrome

(2008) Anna Sarkozy et al.   Orphanet Journal of Rare Diseases