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

PRICKLE1-related early onset epileptic encephalopathy

2018 - AMERICAN JOURNAL OF MEDICAL GENETICS. PART A

Mastrangelo, M; Tolve, M; Martinelli, M; DI NOIA, S; Parrini, E; Leuzzi, V

What is new with 22q? An update from the 22q and You Center at the Children's Hospital of Philadelphia

2018 - AMERICAN JOURNAL OF MEDICAL GENETICS. PART A

Campbell, I. M.; Sheppard, S. E.; Crowley, T. B.; Mcginn, D. E.; Bailey, A.; Mcginn, M. J.; Unolt, M.; Homans, J. F.; Chen, E. Y.; Salmons, H. I.; Gaynor, J. W.; Goldmuntz, E.; Jackson, O. A.; Katz, L. E.; Mascarenhas, M. R.; Deeney, V. F. X.; Castelein, R. M.; Zur, K. B.; Elden, L.; Kallish, S.; Kolon, T. F.; Hopkins, S. E.; Chadehumbe, M. A.; Lambert, M. P.; Forbes, B. J.; Moldenhauer, J. S.; Schindewolf, E. M.; Solot, C. B.; Moss, E. M.; Gur, R. E.; Sullivan, K. E.; Emanuel, B. S.; Zackai, E. H.; McDonald-McGinn, D. 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.