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American Journal of Medical Genetics. Part A|April 18, 2018
Congenital heart diseases and cardiovascular abnormalities in 22q11.2 deletion syndrome: From well-established knowledge to new frontiersMarta Unolt, Paolo Versacci, Silvia Anaclerio, et al.
American Journal of Medical Genetics. Part A|April 23, 2020
Differences in morbidity and mortality in Down syndrome are related to the type of congenital heart defectAnwar Baban, Nicole Olivini, Nicoletta Cantarutti, et al.
The American Journal of Cardiology|August 19, 2007
Prevalence and clinical significance of cardiovascular abnormalities in patients with the LEOPARD syndromeGiuseppe Limongelli, Giuseppe Pacileo, Bruno Marino, et al.
Heart Failure Clinics|November 15, 2021
Hypertrophic Cardiomyopathy in RASopathies: Diagnosis, Clinical Characteristics, Prognostic Implications, and ManagementMichele Lioncino, Emanuele Monda, Federica Verrillo, et al.
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation|June 22, 2018
Risk Score for the Development of Veno-Occlusive Disease after Allogeneic Hematopoietic Cell TransplantChristopher Strouse, Ying Zhang, Mei-Jie Zhang, et al.
American Journal of Medical Genetics. Part A|January 25, 2014
Behavioral profile in RASopathiesPaolo Alfieri, Giorgia Piccini, Cristina Caciolo, et al.
American Journal of Human Genetics|July 26, 2011
Mutations in ANKRD11 cause KBG syndrome, characterized by intellectual disability, skeletal malformations, and macrodontiaAsli Sirmaci, Michail Spiliopoulos, Francesco Brancati, et al.
Brain Sciences|November 14, 2020
7q11.23 Microduplication Syndrome: Clinical and Neurobehavioral ProfilingMaria Lisa Dentici, Paola Bergonzini, Francesco Scibelli, et al.
Archives of Disease in Childhood|October 5, 2014
Kabuki syndrome: clinical and molecular diagnosis in the first year of lifeMaria Lisa Dentici, Alessandra Di Pede, Francesca Romana Lepri, et al.
Plos One|April 2, 2019
Left pulmonary artery in 22q11.2 deletion syndrome. Echocardiographic evaluation in patients without cardiac defects and role of Tbx1 in miceGioia Mastromoro, Giulio Calcagni, Paolo Versacci, et al.
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