Phenotypic heterogeneity in 22q11.2 deletion syndrome: Copy Number Variants as genetic modifiers for congenital heart disease in a Brazilian cohort - Zamariolli, Malu; Dantas, Anelisa Gollo; Nunes, Natália; Moyses-Oliveira, Mariana; Sgardioli, Ilária Cristina; Soares, Diogo Cordeiro de Queiroz; Gil-da-Silva-Lopes, Vera Lúcia; Kim, Chong Ae; Melaragno, Maria Isabel de Souza Aranha (American journal of medical genetics, 2023)