Noonan Syndrome: Clinical Features, Diagnosis, and Management Guidelines

By Alicia A. Romano, J. Allanson, J. Dahlgren, B. Gelb, B. Hall, M. Pierpont, A. Roberts, Wanda Robinson, C. Takemoto, J. Noonan. Pediatrics, 2010

611 citations recorded by the source corpus.

Subfields: Immunology, Molecular Biology, Oncology

View Paper: https://www.semanticscholar.org/paper/925a7045be88f743ffd2e9740b3e70bfe0c2466b

Citations in the corpus

• Recurrent somatic alterations of FGFR1 and NTRK2 in pilocytic astrocytoma (2013, neutral): “Germline PTPN11 mutations are one of the causes of the hereditary developmental disorders Noonan syndrome 44 and multiple lentigines syndrome (also known as LEOPARD syndrome) 45 .”