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- [3] Noonan syndrome: Severe phenotype and PTPN11 mutations MEDICINA CLINICA, 2019, 152 (02): : 62 - 64
- [8] Co-Occurrence of DNET and Lymphoma in a patient with Noonan syndrome and mutation in PTPN11 gene HORMONE RESEARCH IN PAEDIATRICS, 2024, 97 : 413 - 413