MOLINATTO, Cristina
MOLINATTO, Cristina
A familial case of DD/ID variable psychiatric phenotype and optic atrophy due to a novel 1,5 Mb deletion on 2q29
2012-01-01 Belligni E; Biamino E; Molinatto C; Calcia A; Ferrero GB; Silengo M
A rare craniosynostosis associated with an atypical 22q11 microdeletion
2011-01-01 Molinatto C; Belligni E; Biamino E; Gaglini P; Calcia A; Di Gregorio E; Di Rocco C; Silengo M; Brusco A; Ferrero GB
Adult phenotype of Beckwith-Wiedemann syndrome
2019-01-01 Carli, D; Gazzin, A; Molinatto, C; Sirchia, F; Cardaropoli, S; Mussa, A; Ferrero, GB
EXTENSIVE IMMUNOPHENOTYPING IN 22q11 DELETION SYNDROME: DOES B AND T CELLS INFLUENCE CLINICAL HISTORY?
2016-01-01 Licciardi, F.; Franzin, V.; Gallo, E.; Ricotti, E.; Molinatto, C.; Galliano, I.; Bergallo, M.; Santarelli, F.; Ceci, M.; Martino, S.; Montin, D.
Incidence of Beckwith-Wiedemann syndrome
2012-01-01 Molinatto C; Mussa A; De Crescenzo N; Chiesa N; Baldassarre G; Selicorni A; Russo S; Riccio A; Silengo M; Ferrero GB.
Microduplicazione 17p13.1 in un paziente con diabete mellito2, sindrome metabolica e ritardo mentale
2011-01-01 Belligni EF; Di Gregorio E; Biamino E; Molinatto C; Calcia A; Talarico F; Ferrero GB; Brusco A; Silengo M
Phenotype evolution and health issues of adult patients affected by Beckwith-Wiedemann Syndrome
2018-01-01 gazzin andrea, carli diana, molinatto cristina, cardaropoli simona, mussa alessandro, ferrero giovanni battista
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| A familial case of DD/ID variable psychiatric phenotype and optic atrophy due to a novel 1,5 Mb deletion on 2q29 | 2012 | Belligni E; Biamino E; Molinatto C; Calcia A; Ferrero GB; Silengo M | |
| A rare craniosynostosis associated with an atypical 22q11 microdeletion | 2011 | Molinatto C; Belligni E; Biamino E; Gaglini P; Calcia A; Di Gregorio E; Di Rocco C; Silengo M; Brusco A; Ferrero GB | |
| Adult phenotype of Beckwith-Wiedemann syndrome | 2019 | Carli, D; Gazzin, A; Molinatto, C; Sirchia, F; Cardaropoli, S; Mussa, A; Ferrero, GB | |
| EXTENSIVE IMMUNOPHENOTYPING IN 22q11 DELETION SYNDROME: DOES B AND T CELLS INFLUENCE CLINICAL HISTORY? | 2016 | Licciardi, F.; Franzin, V.; Gallo, E.; Ricotti, E.; Molinatto, C.; Galliano, I.; Bergallo, M.; Santarelli, F.; Ceci, M.; Martino, S.; Montin, D. | |
| Incidence of Beckwith-Wiedemann syndrome | 2012 | Molinatto C; Mussa A; De Crescenzo N; Chiesa N; Baldassarre G; Selicorni A; Russo S; Riccio A; Silengo M; Ferrero GB. | |
| Microduplicazione 17p13.1 in un paziente con diabete mellito2, sindrome metabolica e ritardo mentale | 2011 | Belligni EF; Di Gregorio E; Biamino E; Molinatto C; Calcia A; Talarico F; Ferrero GB; Brusco A; Silengo M | |
| Phenotype evolution and health issues of adult patients affected by Beckwith-Wiedemann Syndrome | 2018 | gazzin andrea, carli diana, molinatto cristina, cardaropoli simona, mussa alessandro, ferrero giovanni battista |