Related Articles
Mutational and functional analysis of the BVES gene coding region in Chinese patients with non-syndromic tetralogy of Fallot
MESP1 loss‑of‑function mutation contributes to double outlet right ventricle
Somatic mutations in the GATA6 gene underlie sporadic tetralogy of Fallot
TBX20 loss-of-function mutation contributes to double outlet right ventricle
Somatic GATA5 mutations in sporadic tetralogy of Fallot