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Molecular Cytogenetics|August 15, 2022
Prenatal diagnosis and genetic counseling of an inherited unbalanced chromosome abnormalities in a Chinese familyYing Zhang, Juan Chen, Zonghui Feng, et al.
Frontiers in Genetics|November 20, 2025
Case Report: identification of a novel 9.159-kb deletion in a Chinese α-thalassemia family using single molecule real-time technology sequencingShulin Wu, Zonghui Feng, Fuxiang Jiang, et al.
Advances in Clinical and Experimental Medicine : Official Organ Wroclaw Medical University|May 26, 2025
Importance of single nucleotide polymorphism microarray in prenatal diagnosisZonghui Feng, Yan Chen, Fengmei Yi, et al.
European Journal of Medical Research|August 27, 2025
Identification of a novel POU4F3 frameshift variant in a Chinese family with autosomal dominant hearing lossJie Li, Shengmei Yang, Zonghui Feng, et al.
Frontiers in Genetics|May 24, 2024
206,977 newborn screening results reveal the ethnic differences in the spectrum of inborn errors of metabolism in Huaihua, ChinaGang Xiao, Zonghui Feng, Chaochao Xu, et al.
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