GRILLI, FEDERICO
GRILLI, FEDERICO
Universita' degli Studi di MILANO
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A novel de novo DDX3X missense variant in a female with brachycephaly and intellectual disability : a case report
2021 G. Moresco, J. Costanza, C. Santaniello, O. Rondinone, F. Grilli, E. Prada, S. Orcesi, I. Coro, A. Pichiecchio, P. Marchisio, M. Miozzo, L. Fontana, D. Milani
Let time teach you : A case report of a double diagnosis of 17P duplication and Ehlers-Danlos syndrome
2022 P. Castronovo, S. Aleo, A. Seresini, F. Grilli, E. Brunati, P. Marchisio, S. Guez, D. Milani
Pitfalls of whole exome sequencing in undefined clinical conditions with a suspected genetic etiology
2022 G. Moresco, O. Rondinone, A. Mauri, J. Costanza, C. Santaniello, P. Colapietro, E. Micaglio, G. Marfia, C. Pesenti, F. Grilli, B. Rinaldi, E. Prada, G. Scuvera, R. Villa, M.F. Bedeschi, M.R. Miozzo, D. Milani, L. Fontana
| Titolo | Data di pubblicazione | Autori | Tipo | File | Abstract |
|---|---|---|---|---|---|
| A novel de novo DDX3X missense variant in a female with brachycephaly and intellectual disability : a case report | 31-mar-2021 | Moresco G.Rondinone O.Grilli F.Prada E.Marchisio P.Miozzo M.Fontana L.Milani D. + | Article (author) | - | |
| Let time teach you : A case report of a double diagnosis of 17P duplication and Ehlers-Danlos syndrome | 23-nov-2022 | Aleo, SebastianoGrilli, FedericoMarchisio, Paola + | Article (author) | - | |
| Pitfalls of whole exome sequencing in undefined clinical conditions with a suspected genetic etiology | 1-dic-2022 | Moresco, GiadaRondinone, OrnellaMauri, AlessiaColapietro, PatriziaMarfia, GiovanniGrilli, FedericoRinaldi, BerardoPrada, ElisabettaMiozzo, Monica RosaMilani, DonatellaFontana, Laura + | Article (author) | - |