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Mostrati risultati da 1 a 3 di 3
Moebius syndrome : clinical features, diagnosis, management and early intervention
2016 O. Picciolini, M. Porro, E. Cattaneo, S. Castelletti, G. Masera, F. Mosca, M.F. Bedeschi
Rare interstitial deletion of chromosome 2p11.2p12 : Report of a new patient with developmental delay and unusual clinical features
2016 R. Silipigni, E. Cattaneo, M. Baccarin, M. Fumagalli, M.F. Bedeschi
Currarino syndrome and microcephaly due to a rare 7q36.2 microdeletion: a case report
2018 L. Cococcioni, S. Paccagnini, E. Pozzi, L. Spaccini, E. Cattaneo, S. Redaelli, F. Crosti, G.V. Zuccotti
Titolo | Data di pubblicazione | Autori | Tipo | File | Abstract |
---|---|---|---|---|---|
Moebius syndrome : clinical features, diagnosis, management and early intervention | 2016 | M. PorroE. CattaneoF. Mosca + | Article (author) | - | |
Rare interstitial deletion of chromosome 2p11.2p12 : Report of a new patient with developmental delay and unusual clinical features | 2016 | R. SilipigniE. CattaneoM. BaccarinM. Fumagalli + | Article (author) | - | |
Currarino syndrome and microcephaly due to a rare 7q36.2 microdeletion: a case report | 2018 | Cococcioni, LuciaCattaneo, ElisaREDAELLI, SERENAZuccotti, Gian Vincenzo + | Article (author) | - |
Mostrati risultati da 1 a 3 di 3
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