Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitlePhenotypic heterogeneity in 22q11.2 deletion syndrome: Copy Number Variants as genetic modifiers for congenital heart disease in a Brazilian cohort.AuthorsZamariolli, M.; Dantas, A. G.; Nunes, N.; Moysés‐Oliveira, M.; Sgardioli, I. C.; Soares, D. C. Q.; Gil‐Da‐Silva‐Lopes, V. L.; Kim, C. A.; Melaragno, M. I.PublicationAmerican Journal of Medical Genetics. Part A, 2023, Vol 191, Issue 5, p1273ISSN1552-4825Publication typeArticleDOI10.1002/ajmg.a.63145