Multiple, diffuse schwannomas in a RASopathy phenotype patient with germline KRAS mutation: a causal relationship?

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

Cancer risk in patients with Noonan syndrome carrying a PTPN11 mutation

(2011) Marjolijn C J Jongmans et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Schwannomatosis, sporadic schwannomatosis, and familial schwannomatosis: a surgical series with long-term follow-up

(2010) Augusto Gonzalvo et al.   JOURNAL OF NEUROSURGERY

Craniosynostosis in patients with Noonan syndrome caused by germline KRAS mutations

(2009) Christian P. Kratz et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

The RASopathies: developmental syndromes of Ras/MAPK pathway dysregulation

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

Malignant Diseases in Noonan Syndrome and Related Disorders

(2009) Henrik Hasle   HORMONE RESEARCH

Noonan syndrome caused by germline KRAS mutation in Taiwan: report of two patients and a review of the literature

(2008) Fu-Sung Lo et al.   EUROPEAN JOURNAL OF PEDIATRICS

Evidence of a four-hit mechanism involvingSMARCB1andNF2in schwannomatosis-associated schwannomas

(2007) Roberta Sestini et al.   HUMAN MUTATION