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Heliyon|August 18, 2023
Analysis of potential copy-number variations and genes associated with first-trimester missed abortionWen Zeng, Hong Qi, Yang Du, et al.
DNA and Cell Biology|November 2, 2022
Identification of Diagnostic Variants in FGFR2 and NPR2 Genes in a Chinese Family Affected by Crouzon Syndrome and Acromesomelic Dysplasia, Type MaroteauxJianJiang Zhu, Ran Meng, HuaWei Zhao, et al.
Disease Markers|June 7, 2023
Analysis of 17 Prenatal Cases with the Chromosomal 1q21.1 Copy Number VariationXiaohui Wen, Huanxia Xing, Keyan Qi, et al.
American Journal of Translational Research|April 15, 2022
A familial 3q28q29 duplication induced mild intellectual disability: case presentation and literature reviewXiaohui Wen, Jianjiang Zhu, Lirong Cai, et al.
Molecular Genetics & Genomic Medicine|July 19, 2019
Detection of a rare de novo 18p terminal deletion with inverted duplication in a Chinese pregnant womanJianjiang Zhu, Hong Qi, Sha Cao, et al.
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