| For: | Chen L, Huang FX. Apert syndrome diagnosed by prenatal ultrasound combined with magnetic resonance imaging and whole exome sequencing: A case report. World J Clin Cases 2021; 9(4): 912-918 [PMID: 33585639 DOI: 10.12998/wjcc.v9.i4.912] |
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| URL: | https://www.wjgnet.com/2307-8960/full/v9/i4/912.htm |
| Number | Citing Articles |
| 1 |
Nathan Khabyeh-Hasbani, Yi-Hseuh Lu, William Baumgartner, Shaun D. Mendenhall, Steven M. Koehler. Contemporary Management of the Upper Limb in Apert Syndrome: A Review. Plastic and Reconstructive Surgery - Global Open 2024; 12(8) doi: 10.1097/GOX.0000000000006067
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| 2 |
Guo-Rong Lyu, Shao-Zheng He, Qiu-Xia Jiang, Hai-Bin Lin, Shi-Jie Zhang. Prenatal diagnosis of triphalangeal thumb-polysyndactyly syndrome by ultrasonography combined with genetic testing: A case report. World Journal of Clinical Cases 2021; 9(23): 6832-6838 doi: 10.12998/wjcc.v9.i23.6832
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| 3 |
Xiaoying Chen, Pengzhen Jin, Min Chen, Juan Zuo, Jie Liu, Jin Zhu, Miaochun Lin, Zhaohui Li, Minyue Dong. Prenatal diagnosis of Apert syndrome caused by a de novo FGFR2 mutation in the second trimester: a case report. BMC Pregnancy and Childbirth 2026; 26(1) doi: 10.1186/s12884-026-09282-z
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| 4 |
Dongxue Pan, Xiufang Yang. Identification of a Novel FGFR2 Gene Mutation (c.514_515delinsCT, p.Ala172Leu) in a Chinese Neonate With Apert Syndrome: A Case Report. American Journal of Medical Genetics Part A 2025; 197(11) doi: 10.1002/ajmg.a.64158
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