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Mar 26, 2023 (publication date) through Apr 3, 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: | Shen R, Feng JH, Yang SP. Acromicric dysplasia caused by a mutation of fibrillin 1 in a family: A case report. World J Clin Cases 2023; 11(9): 2036-2042 [PMID: 36998968 DOI: 10.12998/wjcc.v11.i9.2036] |
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| URL: | https://www.wjgnet.com/2307-8960/full/v11/i9/2036.htm |
| Number | Citing Articles |
| 1 |
Fengyan Tian, Xiao Dong, Ruyue Yuan, Xiaohan Hou, Jing Qing, Yani Li. Case Report: Two different acromelic dysplasia phenotypes in a Chinese family caused by a missense mutation in FBN1 and a literature review. Frontiers in Pediatrics 2024; 12 doi: 10.3389/fped.2024.1428513
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