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- [2] Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome Nature Genetics, 2001, 29 : 465 - 468
- [10] Functional analysis of PTPN11/SHP-2 mutants identified in Noonan syndrome and childhood leukemia Journal of Human Genetics, 2005, 50 : 192 - 202