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- European Medical Education Initiative on Noonan syndrome: A clinical practice survey assessing the diagnosis and clinical management of individuals with Noonan syndrome across Europe2022 | 2. lékařská fakulta
- Management of growth failure and other endocrine aspects in patients with Noonan syndrome across Europe: A sub-analysis of a European clinical practice survey2022 | 2. lékařská fakulta
- A restricted spectrum of NRAS mutations causes Noonan syndrome2010 | 2. lékařská fakulta
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- Prenatální fenotyp RASopatií2020 | Publikace bez příslušnosti k fakultě
- The clinical significance of A2ML1 variants in Noonan syndrome has to be reconsidered2021 | 2. lékařská fakulta
- Alterations in key signaling pathways in sinonasal tract melanoma. A molecular genetics and immunohistochemical study of 90 cases and comprehensive review of the literature2022 | Lékařská fakulta v Plzni