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Feb 6, 2023 (publication date) through Mar 28, 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: | Huang TT, Xu HF, Wang SY, Lin WX, Tung YH, Khan KU, Zhang HH, Guo H, Zheng G, Zhang G. Identification of 1q21.1 microduplication in a family: A case report. World J Clin Cases 2023; 11(4): 874-882 [PMID: 36818619 DOI: 10.12998/wjcc.v11.i4.874] |
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| URL: | https://www.wjgnet.com/2307-8960/full/v11/i4/874.htm |
| Number | Citing Articles |
| 1 |
Fengyang Wang, Huijuan Peng, Guiyu Lou, Yanxin Ren, Shixiu Liao. Prenatal ultrasound phenotype of fetuses with recurrent 1q21.1 deletion and duplication syndrome. Frontiers in Pediatrics 2025; 12 doi: 10.3389/fped.2024.1504122
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| 2 |
Cuiting Peng, Han Chen, Fan Zhou, Hong Yang, Yutong Li, Yuezhi Keqie, Xu Zhao, He Wang, Ting Hu, Shanling Liu, Jun Ren, Xinlian Chen. Molecular diagnosis and preimplantation genetic testing for chromosome 1q21.1 recurrent microduplication. Frontiers in Genetics 2025; 16 doi: 10.3389/fgene.2025.1522406
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| 3 |
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| 4 |
Behjat Ul Mudassir, Mashael Alhumaidi Alotaibi, Nadeem Kizilbash, Daliyah Alruwaili, Anwar Alruwaili, Modhi Alenezi, Zehra Agha. Genome-wide CNV analysis uncovers novel pathogenic regions in cohort of five multiplex families with neurodevelopmental disorders. Heliyon 2023; 9(9): e19718 doi: 10.1016/j.heliyon.2023.e19718
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