Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Stefania Cavone"'
Autor:
Valentina Pinna, Paola Daniele, Giulio Calcagni, Lucio Mariniello, Roberta Criscione, Chiara Giardina, Francesca Romana Lepri, Hossein Hozhabri, Angela Alberico, Stefania Cavone, Annunziata Tina Morella, Roberta Mandile, Francesca Annunziata, Niccolò Di Giosaffatte, Maria Cecilia D’Asdia, Paolo Versacci, Rossella Capolino, Pietro Strisciuglio, Sandra Giustini, Daniela Melis, Maria Cristina Digilio, Marco Tartaglia, Bruno Marino, Alessandro De Luca
Publikováno v:
Genes, Vol 10, Iss 9, p 675 (2019)
The aim of this study was to assess the prevalence and type of congenital heart disease (CHD) and the associated mutation spectrum in a large series of patients with neurofibromatosis type 1 (NF1), and correlate the mutation type with the presence an
Externí odkaz:
https://doaj.org/article/fd8483b3d5e14404b7f5d130dbf395dd
Autor:
Annunziata Morella, Francesca Romana Lepri, Lucio Mariniello, Sandra Giustini, Maria Cecilia D'Asdia, Maria Cristina Digilio, Marco Tartaglia, Roberta Mandile, Valentina Pinna, Chiara Giardina, Roberta Criscione, Pietro Strisciuglio, Niccolò Di Giosaffatte, Paolo Versacci, Angela Alberico, Alessandro De Luca, Stefania Cavone, Hossein Hozhabri, Daniela Melis, Rossella Capolino, Giulio Calcagni, Bruno Marino, Paola Daniele, F. Annunziata
Publikováno v:
Genes
Genes, Vol 10, Iss 9, p 675 (2019)
Volume 10
Issue 9
Genes, Vol 10, Iss 9, p 675 (2019)
Volume 10
Issue 9
The aim of this study was to assess the prevalence and type of congenital heart disease (CHD) and the associated mutation spectrum in a large series of patients with neurofibromatosis type 1 (NF1), and correlate the mutation type with the presence an