Malignancy in Noonan syndrome and related disorders
Author:
Affiliation:
1. Division of Genetics & Metabolism; Children's National Health System; Washington D.C. USA
2. Department of Pediatrics; The George Washington University School of Medicine & Health Sciences; Washington D.C. USA
Publisher
Wiley
Subject
Genetics (clinical),Genetics
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4. Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP2, cause Noonan syndrome;Tartaglia;Nat Genet,2001
5. Germline gain-of-function mutations in SOS1 cause Noonan syndrome;Roberts;Nat Genet,2007
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