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Jul 26, 2022 (publication date) through Sep 10, 2025
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Publication Name
World Journal of Clinical Cases
ISSN
2307-8960
Publisher of This Article
Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
| 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] |
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| URL: | https://www.wjgnet.com/2307-8960/full/v10/i21/7517.htm |
| Number | Citing Articles |
| 1 |
Silvana Bochicchio, Aurora Mazzetti, Lorenzo Graziani, Gian Gaetano Tartaglia, Stefano Gustincich, Remo Sanges. Molecular features of AHDC1: insights into an overlooked gene with broad functional potential. Human Genetics 2025; doi: 10.1007/s00439-025-02765-7
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| 2 |
Nan Jiang, Liyuan Zhang, Zeyan Zheng, Hanze Du, Shi Chen, Hui Pan. Phenotypic subtypes of Xia-Gibbs syndrome: a latent class analysis. European Journal of Human Genetics 2024; doi: 10.1038/s41431-024-01754-0
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| 3 |
Nan Jiang, Liyuan Zhang, Zeyan Zheng, Hanze Du, Shi Chen, Hui Pan. Correction: Phenotypic subtypes of Xia-Gibbs syndrome: a latent class analysis. European Journal of Human Genetics 2025; doi: 10.1038/s41431-025-01825-w
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