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Dec 26, 2020 (publication date) through Jun 8, 2024
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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: | Li JR, Huang Z, Lu Y, Ji QY, Jiang MY, Yang F. Novel mutation in the ASXL3 gene in a Chinese boy with microcephaly and speech impairment: A case report. World J Clin Cases 2020; 8(24): 6465-6472 [PMID: 33392332 DOI: 10.12998/wjcc.v8.i24.6465] |
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| URL: | https://www.wjgnet.com/2307-8960/full/v8/i24/6465.htm |
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| 2 |
Qin Wang, Jianming Zhang, Nan Jiang, Jiansheng Xie, Jingxin Yang, Xiaoshan Zhao. De novo nonsense variant in ASXL3 in a Chinese girl causing Bainbridge–Ropers syndrome: A case report and review of literature. Molecular Genetics & Genomic Medicine 2022; 10(5) doi: 10.1002/mgg3.1924
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| 3 |
Emily Woods, Nicola Holmes, Shadi Albaba, Iwan R. Evans, Meena Balasubramanian. ASXL3‐related disorder: Molecular phenotyping and comprehensive review providing insights into disease mechanism. Clinical Genetics 2024; 105(5): 470 doi: 10.1111/cge.14506
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