Crossref Citations
This article has been cited by the following publications. This list is generated based on data provided by Crossref.
Calcagni, Giulio
Unolt, Marta
Digilio, Maria Cristina
Baban, Anwar
Versacci, Paolo
Tartaglia, Marco
Baldini, Antonio
and
Marino, Bruno
2017.
Congenital heart disease and genetic syndromes: new insights into molecular mechanisms.
Expert Review of Molecular Diagnostics,
Vol. 17,
Issue. 9,
p.
861.
Unolt, Marta
Versacci, Paolo
Anaclerio, Silvia
Lambiase, Caterina
Calcagni, Giulio
Trezzi, Matteo
Carotti, Adriano
Crowley, Terrence Blaine
Zackai, Elaine H.
Goldmuntz, Elizabeth
Gaynor, James William
Digilio, Maria Cristina
McDonald‐McGinn, Donna M.
and
Marino, Bruno
2018.
Congenital heart diseases and cardiovascular abnormalities in 22q11.2 deletion syndrome: From well‐established knowledge to new frontiers.
American Journal of Medical Genetics Part A,
Vol. 176,
Issue. 10,
p.
2087.
Unolt, Marta
Calcagni, Giulio
Putotto, Carolina
Versacci, Paolo
Digilio, Maria Cristina
and
Marino, Bruno
2022.
The Chromosome 22q11.2 Deletion Syndrome.
p.
78.
Putotto, Carolina
Pugnaloni, Flaminia
Unolt, Marta
Maiolo, Stella
Trezzi, Matteo
Digilio, Maria Cristina
Cirillo, Annapaola
Limongelli, Giuseppe
Marino, Bruno
Calcagni, Giulio
and
Versacci, Paolo
2022.
22q11.2 Deletion Syndrome: Impact of Genetics in the Treatment of Conotruncal Heart Defects.
Children,
Vol. 9,
Issue. 6,
p.
772.
Cirillo, Annapaola
Lioncino, Michele
Maratea, Annachiara
Passariello, Annalisa
Fusco, Adelaide
Fratta, Fiorella
Monda, Emanuele
Caiazza, Martina
Signore, Giovanni
Esposito, Augusto
Baban, Anwar
Versacci, Paolo
Putotto, Carolina
Marino, Bruno
Pignata, Claudio
Cirillo, Emilia
Giardino, Giuliana
Sarubbi, Berardo
Limongelli, Giuseppe
and
Russo, Maria Giovanna
2022.
Clinical Manifestations of 22q11.2 Deletion Syndrome.
Heart Failure Clinics,
Vol. 18,
Issue. 1,
p.
155.