Wanqin Xie
8PUBLICATIONS
5CO-AUTHORS
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Publications (8)
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|Dec 11, 2025
Identification of a Novel Splice-Site Variant in CACNA1F With Variable Phenotypic Expression in a Chinese Family.Mojiang Li, Cheng Chen, Yingshu Li
|Jun 16, 2025
Compound Heterozygous Loss-of-Function Variants in CCM2L in a Fetus With Tetralogy of Fallot.Dandan Ling, Wanqin Xie, Xiao Mao
|Aug 23, 2024
Clinical features of a novel compound heterozygous genotype of the BBS2 gene: a case report.Mojiang Li, Yingshu Li, Ting Wen
|Apr 08, 2024
Compound heterozygous B3GALNT2 mutations in a fetus with encephalocele: A case report.Dandan Ling, Wanqin Xie, Xiao Mao
|May 31, 2021
Implementation of fragile X syndrome carrier screening during prenatal diagnosis: A pilot study at a single center.Hui Xi, Wanqin Xie, Jing Chen
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