Pubblicazioni

Congenital heart diseases and cardiovascular abnormalities in 22q11.2 deletion syndrome: From well-established knowledge to new frontiers

2018 - AMERICAN JOURNAL OF MEDICAL GENETICS. PART A

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.; Marino, Bruno

Genetic and clinical features of social cognition in 22q11.2 deletion syndrome

2018 - JOURNAL OF NEUROSCIENCE RESEARCH

Lattanzi, Guido Maria; Buzzanca, Antonino; Frascarelli, Marianna; DI FABIO, Fabio

Primary lymphedema and other lymphatic anomalies are associated with 22q11.2 deletion syndrome

2018 - EUROPEAN JOURNAL OF MEDICAL GENETICS

Unolt, Marta; Barry, Jessica; Digilio, Maria Cristina; Marino, Bruno; Bassett, Anne; Oechslin, Erwin; Low, David W.; Belasco, Jean B.; Kallish, Staci; Sullivan, Kathleen; Zackai, Elaine H.; McDonald-McGinn, Donna M.

22q and two: 22q11.2 deletion syndrome and coexisting conditions

2018 - AMERICAN JOURNAL OF MEDICAL GENETICS. PART A

Cohen, J. L.; Crowley, T. B.; Mcginn, D. E.; Mcdougall, C.; Unolt, M.; Lambert, M. P.; Emanuel, B. S.; Zackai, E. H.; McDonald-McGinn, D. M.