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Cited by in CrossRef
For: Lin SZ, Xie HY, Qu YL, Gao W, Wang WQ, Li JY, Feng XC, Jin CQ. Novel frameshift mutation in the AHDC1 gene in a Chinese global developmental delay patient: A case report. World J Clin Cases 2022; 10(21): 7517-7522 [PMID: 36157999 DOI: 10.12998/wjcc.v10.i21.7517]
URL: https://www.wjgnet.com/2307-8960/full/v10/i21/7517.htm
Number Citing Articles
1
Nan Jiang, Liyuan Zhang, Zeyan Zheng, Hanze Du, Shi Chen, Hui Pan. Phenotypic subtypes of Xia-Gibbs syndrome: a latent class analysisEuropean Journal of Human Genetics 2024;  doi: 10.1038/s41431-024-01754-0
2
Nan Jiang, Liyuan Zhang, Zeyan Zheng, Hanze Du, Shi Chen, Hui Pan. Correction: Phenotypic subtypes of Xia-Gibbs syndrome: a latent class analysisEuropean Journal of Human Genetics 2025;  doi: 10.1038/s41431-025-01825-w