A case of polimalformed fetus with a microdeletion of CTNNA3 gene

Por Cancemi, Dino, Urciuoli, Maria, Morelli, Franco, Lonardo, Maria Concetta, Lonardo, Valeria, Spampanato, Carmine, Ventruto, Marialuisa, Ventruto, Valerio, Sica, Carmine
Publicado no J Prenat Med (2016)

Congenital megaurethra in a fetus with Meckel syndrome and in a fetus with female pseudoermanphroditism. The first report of these occurrences

Por Di Meglio, Letizia, Mazzarelli, Laura Letizia, Boscaino, Amedeo, Cancemi, Dino, Morelli, Franco, Lonardo, Maria Concetta, Lonardo, Valeria, Friso, Patrizia, Spampanato, Carmine, Urciuoli, Maria, Ventruto, Marialuisa, Ventruto, Valerio
Publicado no J Prenat Med (2014)

Investigating the role of X chromosome breakpoints in premature ovarian failure

Por Baronchelli Simona, Villa Nicoletta, Redaelli Serena, Lissoni Sara, Saccheri Fabiana, Panzeri Elena, Conconi Donatella, Bentivegna Angela, Crosti Francesca, Sala Elena, Bertola Francesca, Marozzi Anna, Pedicini Antonio, Ventruto Marialuisa, Police Maria, Dalprà Leda
Publicado em 2012-07-01

Investigating the role of X chromosome breakpoints in premature ovarian failure

Por Baronchelli, Simona, Villa, Nicoletta, Redaelli, Serena, Lissoni, Sara, Saccheri, Fabiana, Panzeri, Elena, Conconi, Donatella, Bentivegna, Angela, Crosti, Francesca, Sala, Elena, Bertola, Francesca, Marozzi, Anna, Pedicini, Antonio, Ventruto, Marialuisa, Police, Maria Adalgisa, Dalprà, Leda
Publicado em 2012