Associated Papers
Analysis of pathogenic variants in 605 Chinese children with non-syndromic cardiac conotruncal defects based on targeted sequencing.
Ye J et al.
Genomics, 2023
Phenotypic spectrum of FGF10-related disorders: a systematic review.
Bzdega K et al.
Peerj, 2022
Mutations in fibroblast growth factor (FGF8) and FGF10 identified in patients with conotruncal defects.
Zhou S et al.
Journal of Translational Medicine, 2020
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