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UnknownClinical and Molecular Findings of Tunisian Patients with RASopathies.
Not available
S-EPMC4188152 | biostudies-literature
UnknownGenotype and phenotype spectrum of NRAS germline variants.
Not available
S-EPMC5520077 | biostudies-literature
UnknownCancer spectrum and frequency among children with Noonan, Costello, and cardio-facio-cutaneous syndromes.
Not available
S-EPMC4402457 | biostudies-literature
UnknownThe clinical significance of A2ML1 variants in Noonan syndrome has to be reconsidered.
Not available
S-EPMC7940614 | biostudies-literature
UnknownActivating Mutations Affecting the Dbl Homology Domain of SOS2 Cause Noonan Syndrome.
Not available
S-EPMC4604019 | biostudies-literature
UnknownVariants of SOS2 are a rare cause of Noonan syndrome with particular predisposition for lymphatic complications.
Not available
S-EPMC7852574 | biostudies-literature
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