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- [42] Clinical and Genetic Characteristics of Noonan Syndrome and Noonan-like Diseases Russian Journal of Genetics, 2020, 56 : 540 - 547
- [43] Mutations in PTPN11 could lead to a congenital myasthenic syndrome phenotype: a Noonan syndrome case series Journal of Neurology, 2024, 271 : 1331 - 1341
- [44] The Fetal Phenotype of Noonan Syndrome Caused by Severe, Cancer-Related PTPN11 Variants AMERICAN JOURNAL OF CASE REPORTS, 2020, 21 : e922468 - 1
- [50] Phenotypic differences in Noonan syndrome based on PTPN11 mutation status HORMONE RESEARCH IN PAEDIATRICS, 2023, 96 : 304 - 305