TOLVA, GIANLUCA
TOLVA, GIANLUCA
Universita' degli Studi di MILANO
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Risultati 1 - 4 di 4 (tempo di esecuzione: 0.0 secondi).
Complex genomic alterations and intellectual disability: an interpretative challenge
2020 R. Silipigni, D. Milani, G. Tolva, E. Monfrini, A. Giacobbe, P.G. Marchisio, S. Guerneri
Unexpected phenotype in a frameshift mutation of PTCH1
2020 B. Beltrami, E. Prada, G. Tolva, G. Scuvera, R. Silipigni, D. Graziani, G. Bulfamante, C. Gervasini, P. Marchisio, D. Milani
Mayer–Rokitansky–Küster–Hauser Syndrome and 16p11.2 Recurrent Microdeletion: A Case Report and Review of the Literature
2018 M. Gatti, G. Tolva, S. Bergamaschi, C. Giavoli, S. Esposito, P. Marchisio, D. Milani
Perthes disease : A new finding in Floating-Harbor syndrome
2018 D. Milani, G. Scuvera, M. Gatti, G. Tolva, F. Bonarrigo, S. Esposito, C. Gervasini
| Titolo | Data di pubblicazione | Autori | Tipo | File | Abstract |
|---|---|---|---|---|---|
| Complex genomic alterations and intellectual disability: an interpretative challenge | 2020 | Silipigni R.Milani D.Tolva G.Monfrini E.Marchisio P. G. + | Article (author) | - | |
| Unexpected phenotype in a frameshift mutation of PTCH1 | 2020 | BELTRAMI, BENEDETTAPrada E.Tolva G.Silipigni R.Bulfamante G.Gervasini C.Marchisio P.Milani D. + | Article (author) | - | |
| Mayer–Rokitansky–Küster–Hauser Syndrome and 16p11.2 Recurrent Microdeletion: A Case Report and Review of the Literature | 2018 | Gatti, MartaTolva, GianlucaBergamaschi, SilviaGiavoli, ClaudiaMarchisio, PaolaMilani, Donatella + | Article (author) | - | |
| Perthes disease : A new finding in Floating-Harbor syndrome | 2018 | D. MilaniG. ScuveraGATTI, MARTATOLVA, GIANLUCAF. BonarrigoS. EspositoC. Gervasini | Article (author) | - |