BALDASSARRE, GIUSEPPINA
BALDASSARRE, GIUSEPPINA
a microduplication of the centromeric domain of the 11p15.5 impirnted gene cluster is associated with loss of DNA methylation and familial BWS.
2010-01-01 Chiesa N; De Crescenzo N; Mussa A; Baldassarre G; Perone L; Carella M; Cirillo Silengo M; Riccio A; Ferrero GB
Analisi del profilo di trascrizione genetica nella sindrome di Noonan.
2010-01-01 Picco G; Cantarella D; Baldassarre G; Marinosci A; Dotta A; Isella C; Crescenzo N; Timeus F; Chiesa N; Merla G; Mazzanti L; Rossi C; Zampino G; Tartaglia M; Silengo M; Medico E; Ferrero GB.
Array-CGH analysis in a patient with Acrocallosal Syndrome
2009-01-01 Belligni EF; Ferrero GB; Vetro A; Chiesa N; Biamino E; Molinatto C; Baldassarre G; Zuffardi O; Silengo M
Clinical and molecular characterization of a cohort of 49 children affected by Beckwith-Wiedemann Syndrome and related congenital defects
2008-01-01 Mussa A; Baldassarre G; Molinatto C; Peruzzi L; Pepe E; Riccio A; Cirillo Silengo M
Due nuove mutazioni di PTPN11 nella sindrome di Noonan
2006-01-01 Rossi C; Ferrari S; Ferrero GB; Delmonaco G; Baldassarre G; Belligni E; Banaudi E; Silengo M
Extreme clinical variability in Noonan syndrome with loose anagen hair due to Ser2Gly SHOC mutation
2012-01-01 Baldassarre G; Rossi C; Tartaglia M; Silengo M; Ferrero GB.
Genotypic and phenotypic spectrum of 44 patients with Noonan syndrome
2009-01-01 Baldassarre G; Rossi C; Chiesa N; Mussa A; Marinosci A; Tartaglia M; Silengo M; Ferrero GB
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.
Molecular and clinical characterization of 37 patients with Noonan syndrome
2009-01-01 Baldassarre G; Rossi C; Tartaglia M; Carta C; Banaudi E; Chiesa N; Silengo MC; Ferrero GB
Molecular dissection of Noonan syndrome by transcriptiome analysis
2009-01-01 Ferrero GB; Cantarella D; Baldassarre G; Isella C; Crescenzo N; Timeus F; Chiesa N; Merla G; Mazzanti L; Rossi C; Zampino G; Tartaglia M; Silengo M; Medico E
Myhre syndrome. report of three unrelated patients
2010-01-01 Belligni E; Biamino E; Molinatto C;Baldassarre G; Marinosci A; Ferrero GB; Silengo M
Transcriptional hallmarks of Noonan syndrome in peripheral blood mononuclear cells
2009-01-01 Ferrero GB; Cantarella D; Baldassarre G; Isella C; Crescenzio N; Pagliano S; Silengo M; Medico E
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| a microduplication of the centromeric domain of the 11p15.5 impirnted gene cluster is associated with loss of DNA methylation and familial BWS. | 2010 | Chiesa N; De Crescenzo N; Mussa A; Baldassarre G; Perone L; Carella M; Cirillo Silengo M; Riccio A; Ferrero GB | |
| Analisi del profilo di trascrizione genetica nella sindrome di Noonan. | 2010 | Picco G; Cantarella D; Baldassarre G; Marinosci A; Dotta A; Isella C; Crescenzo N; Timeus F; Chiesa N; Merla G; Mazzanti L; Rossi C; Zampino G; Tartaglia M; Silengo M; Medico E; Ferrero GB. | |
| Array-CGH analysis in a patient with Acrocallosal Syndrome | 2009 | Belligni EF; Ferrero GB; Vetro A; Chiesa N; Biamino E; Molinatto C; Baldassarre G; Zuffardi O; Silengo M | |
| Clinical and molecular characterization of a cohort of 49 children affected by Beckwith-Wiedemann Syndrome and related congenital defects | 2008 | Mussa A; Baldassarre G; Molinatto C; Peruzzi L; Pepe E; Riccio A; Cirillo Silengo M | |
| Due nuove mutazioni di PTPN11 nella sindrome di Noonan | 2006 | Rossi C; Ferrari S; Ferrero GB; Delmonaco G; Baldassarre G; Belligni E; Banaudi E; Silengo M | |
| Extreme clinical variability in Noonan syndrome with loose anagen hair due to Ser2Gly SHOC mutation | 2012 | Baldassarre G; Rossi C; Tartaglia M; Silengo M; Ferrero GB. | |
| Genotypic and phenotypic spectrum of 44 patients with Noonan syndrome | 2009 | Baldassarre G; Rossi C; Chiesa N; Mussa A; Marinosci A; Tartaglia M; Silengo M; Ferrero GB | |
| 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. | |
| Molecular and clinical characterization of 37 patients with Noonan syndrome | 2009 | Baldassarre G; Rossi C; Tartaglia M; Carta C; Banaudi E; Chiesa N; Silengo MC; Ferrero GB | |
| Molecular dissection of Noonan syndrome by transcriptiome analysis | 2009 | Ferrero GB; Cantarella D; Baldassarre G; Isella C; Crescenzo N; Timeus F; Chiesa N; Merla G; Mazzanti L; Rossi C; Zampino G; Tartaglia M; Silengo M; Medico E | |
| Myhre syndrome. report of three unrelated patients | 2010 | Belligni E; Biamino E; Molinatto C;Baldassarre G; Marinosci A; Ferrero GB; Silengo M | |
| Transcriptional hallmarks of Noonan syndrome in peripheral blood mononuclear cells | 2009 | Ferrero GB; Cantarella D; Baldassarre G; Isella C; Crescenzio N; Pagliano S; Silengo M; Medico E |