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Mostrati risultati da 1 a 6 di 6
A rare de novo insertion of Alu element in Fibroblast Growth Factor Receptor 2 (FGFR2) causing Apert syndrome with a different pathologic mechanism
2023/2024 GRAVINA, ELISA
Analysis of putative splicing mutations in human diseases by Minigene assay and reverse transcription-PCR
2020/2021 SPAGLIARDI, ARIANNA
Anomalie controverse del miocardio: studio genetico del ventricolo sinistro non compattato (LVNC)
2023/2024 GIANTOMASSI, MARIA LAURA
Investigating genetic analyses to diagnose patients with neurodevelopmental diseases who tested negative for exome sequencing
2022/2023 PINTUS, FRANCESCO
Rianalisi dei dati esomici in pazienti con malattie del neurosviluppo
2023/2024 SICILIANO, CRISTIAN
UBE2I: a novel gene implicating the SUMOylation pathway in syndromic neurodevelopmental disorders.
2023/2024 AULINO, ALESSANDRA
Mostrati risultati da 1 a 6 di 6
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