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Aug 26, 2021 (publication date) through Nov 5, 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: | Tao Y, Wei Q, Chen X, Nong GM. Geleophysic dysplasia caused by a mutation in FBN1: A case report. World J Clin Cases 2021; 9(24): 7175-7180 [PMID: 34540975 DOI: 10.12998/wjcc.v9.i24.7175] |
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| URL: | https://www.wjgnet.com/2307-8960/full/v9/i24/7175.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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| 2 |
Yuya Komori, Naoki Wada, Yuta Kuwahara, Tsubasa Furuya, Yukihiro Takahashi. Valve Replacement for Progressive Mitral Valve Stenosis Associated with Geleophysic Dysplasia. Japanese Journal of Cardiovascular Surgery 2022; 51(4): 204 doi: 10.4326/jjcvs.51.204
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| 3 |
Tarik Duzenli, Betul Seher Uysal, Berkay Ulas, Gulsum Kayhan.
Geleophysic dysplasia and Weill–Marchesani syndrome:
ADAMTSL2
a possible common gene
. Ophthalmic Genetics 2024; 45(5): 499 doi: 10.1080/13816810.2024.2358973
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