New PRSS1 and common CFTR mutations in a child with acute recurrent pancreatitis, could be considered an "Hereditary" form of pancreatitis ?

Por Corleto, Vito D, Gambardella, Stefano, Gullotta, Francesca, D'Apice, Maria R, Piciucchi, Matteo, Galli, Elena, Lucidi, Vincenzina, Novelli, Giuseppe, Fave, Gianfranco Delle
Publicado em 2010

Prenatal diagnosis of genomic disorders and chromosome abnormalities using array-based comparative genomic hybridization

Por Gullotta, Francesca, Biancolella, Michela, Costa, Elena, Colapietro, Isabella, Nardone, Anna Maria, Molinaro, Paolo, Pietropolli, Adalgisa, Narcisi, Marianovella, Di Rosa, Cristiana, Novelli, Giuseppe
Publicado em 2007

Design, Construction and Validation of Targeted BAC Array-Based CGH Test for Detecting the Most Commons Chromosomal Abnormalities

Por Gambardella, Stefano, Ciabattoni, Erika, Motta, Francesca, Stoico, Giusy, Gullotta, Francesca, Biancolella, Michela, Nardone, Anna Maria, Novelli, Antonio, Brunetti, Ercole, Bernardini, Laura, Novelli, Giuseppe
Publicado no Genomics Insights (2010)

Deletion of REXO1L1 locus in a patient with malabsorption syndrome, growth retardation, and dysmorphic features: a novel recognizable microdeletion syndrome?

Por D’Apice, Maria Rosaria, Novelli, Antonio, di Masi, Alessandra, Biancolella, Michela, Antoccia, Antonio, Gullotta, Francesca, Licata, Norma, Minella, Daniela, Testa, Barbara, Nardone, Anna Maria, Palmieri, Giampiero, Calabrese, Emma, Biancone, Livia, Tanzarella, Caterina, Frontali, Marina, Sangiuolo, Federica, Novelli, Giuseppe, Pallone, Francesco
Publicado no BMC Med Genet (2015)