TOLVA, GIANLUCA
TOLVA, GIANLUCA
Universita' degli Studi di MILANO
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Risultati 1 - 4 di 4 (tempo di esecuzione: 0.0 secondi).
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
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
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 |
---|---|---|---|---|---|
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) | - | |
Complex genomic alterations and intellectual disability: an interpretative challenge | 2020 | Silipigni R.Milani D.Tolva G.Monfrini E.Marchisio P. G. + | 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) | - |