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
Perthes disease : A new finding in Floating-Harbor syndrome
2018 D. Milani, G. Scuvera, M. Gatti, G. Tolva, F. Bonarrigo, S. Esposito, C. Gervasini
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
| 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) | - | |
| Perthes disease : A new finding in Floating-Harbor syndrome | 2018 | D. MilaniG. ScuveraGATTI, MARTATOLVA, GIANLUCAF. BonarrigoS. EspositoC. Gervasini | 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) | - |