Rang Xu
3PUBLICATIONS
2CO-AUTHORS
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Publications (3)
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|Dec 02, 2022
LOF variants identifying candidate genes of laterality defects patients with congenital heart disease.Sijie Liu, Wei Wei, Pengcheng Wang
|Aug 07, 2021
Genetic and functional analyses detect one pathological NFATC1 mutation in a Chinese tricuspid atresia family.Bojian Li, Tingting Li, Tian Pu
|Feb 01, 2020
Identification of FOXH1 mutations in patients with sporadic conotruncal heart defect.Wei Wei, Bojian Li, Fen Li
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