Search

Author/Creator Inzana, Francesca

1. Clinical aspects of Fanconi anemia individuals with the same mutation of FANCF identified by next generation sequencing. Issue 12 (2nd June 2015)

Authors:
Nicchia, Elena; Benedicenti, Francesco; Rocco, Daniela De; Greco, Chiara; Bottega, Roberta; Inzana, Francesca; Faleschini, Michela; Bonin, Serena; Cappelli, Enrico; Mogni, Massimo; Stanzial, Franco; Svahn, Johanna; Dufour, Carlo; Savoia, Anna
Journal:
Birth defects research
Issue:
Volume 103:Issue 12(2015)
Page Start:
1003
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

2. Defining the phenotype associated with microduplication reciprocal to Sotos syndrome microdeletion. Issue 8 (12th May 2014)

Authors:
Novara, Francesca; Stanzial, Franco; Rossi, Elena; Benedicenti, Francesco; Inzana, Francesca; Di Gregorio, Eleonora; Brusco, Alfredo; Graakjaer, Jesper; Fagerberg, Christina; Belligni, Elga; Silengo, Margherita; Zuffardi, Orsetta; Ciccone, Roberto
Journal:
American journal of medical genetics
Issue:
Volume 164:Issue 8(2014.)
Page Start:
2084
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

3. Delineation of the clinical profile of CNOT2 haploinsufficiency and overview of the IDNADFS phenotype. Issue 2 (24th November 2022)

Authors:
Niceta, Marcello; Pizzi, Simone; Inzana, Francesca; Peron, Angela; Bakhtiari, Somayeh; Nizon, Mathilde; Levy, Jonathan; Mancini, Cecilia; Cogné, Benjamin; Radio, Francesca Clementina; Agolini, Emanuele; Cocciadiferro, Dario; Novelli, Antonio; Salih, Mustafa A.; Recalcati, Maria Paola; Arancio, Ro...
Journal:
Clinical genetics
Issue:
Volume 103:Issue 2(2023)
Page Start:
156
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗