Oculoectodermal syndrome is a mosaic RASopathy associated withKRASalterations

Oculoectodermal syndrome: Report of a new case with a broad clinical spectrum

(2014) Deniz Aslan et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

RAS diseases in children

(2014) C. M. Niemeyer   HAEMATOLOGICA

Malignant transformation of infantile hemangioma to angiosarcoma: Response to chemotherapy with bevacizumab

(2014) Michael R. Jeng et al.   PEDIATRIC BLOOD & CANCER

The RASopathies

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

Jaffe–Campanacci syndrome, revisited: detailed clinical and molecular analyses determine whether patients have neurofibromatosis type 1, coincidental manifestations, or a distinct disorder

(2013) Douglas R. Stewart et al.   GENETICS IN MEDICINE

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

Mosaic Activating RAS Mutations in Nevus Sebaceus and Nevus Sebaceus Syndrome

(2012) Bryan K. Sun et al.   JOURNAL OF INVESTIGATIVE DERMATOLOGY

Keratinocytic epidermal nevi are associated with mosaicRASmutations

(2012) Christian Hafner et al.   JOURNAL OF MEDICAL GENETICS

An integrated map of genetic variation from 1,092 human genomes

(2012)   NATURE

Postzygotic HRAS and KRAS mutations cause nevus sebaceous and Schimmelpenning syndrome

(2012) Leopold Groesser et al.   NATURE GENETICS

Oculoectodermal syndrome with coarctation of the aorta and moyamoya disease: Expanding the phenotype to include vascular anomalies

(2011) Liran Horev et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Oculo-ectodermal syndrome: Report of a case with mosaicism for a deletion on Xq12

(2011) Matthew R. Fickie et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Cancer in Noonan, Costello, cardiofaciocutaneous and LEOPARD syndromes

(2011) Christian P. Kratz et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS

Progressive Growth in Epibulbar Complex Choristomas: Report of 2 Cases and Review of Literature

(2011) Valerie Trubnik et al.   CORNEA

Autoimmune lymphoproliferative syndrome-like disease with somatic KRAS mutation

(2010) M. Takagi et al.   BLOOD

Mosaicism for oncogenic G12D KRAS mutation associated with epidermal nevus, polycystic kidneys and rhabdomyosarcoma

(2010) F. Bourdeaut et al.   JOURNAL OF MEDICAL GENETICS

Selective cytotoxicity of a bicyclic Ras inhibitor in cancer cells expressing K-RasG13D

(2009) Alessandro Palmioli et al.   BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS

The RASopathies: developmental syndromes of Ras/MAPK pathway dysregulation

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

Encephalocraniocutaneous lipomatosis

(2009) U Moog   JOURNAL OF MEDICAL GENETICS

Frequency and type of KRAS mutations in routine diagnostic analysis of metastatic colorectal cancer

(2009) Jens Neumann et al.   PATHOLOGY RESEARCH AND PRACTICE

Multiple giant cell lesions in patients with Noonan syndrome and cardio-facio-cutaneous syndrome

(2008) Thomas E Neumann et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

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

(2008) Yoko Aoki et al.   HUMAN MUTATION