Whole-exome sequencing reveals a monogenic cause in 56% of individuals with laterality disorders and associated congenital heart defects.
J Med Genet. 2021 Jul 2:jmedgenet-2021-107775. doi: 10.1136/jmedgenet-2021-107775. Online ahead of print.
J Med Genet. 2021.
PMID: 34215651