BALDASSARRE, GIUSEPPINA

BALDASSARRE, GIUSEPPINA  

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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