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Dive into the research topics of 'A PTPN11 allele encoding a catalytically impaired SHP2 protein in a patient with a Noonan syndrome phenotype'. Together they form a unique fingerprint.- Sort by
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Jonathan J. Edwards, Simone Martinelli, Luca Pannone, Ivan Fai Man Lo, Lisong Shi, Lisa Edelmann, Marco Tartaglia, Ho Ming Luk, Bruce D. Gelb
Research output: Contribution to journal › Article › peer-review