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Year | Number of Results |
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2022 | 1 |
2024 | 2 |
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Page 1
Diagnosis and treatment of the Ehlers-Danlos syndromes in China: synopsis of the first guidelines.
Orphanet J Rare Dis. 2024 May 13;19(1):194. doi: 10.1186/s13023-024-03121-0.
Orphanet J Rare Dis. 2024.
PMID: 38741208
Free PMC article.
Activating PIK3CA postzygotic mutations in segmental overgrowth of muscles with bone involvement in the body extremities.
Tian W, Sun L, Zhang Q, Zhao J, Guo Y, Zhong W, Liu L, Meirelles K, Tang S, Zhang J, Huang Y, Yin Y, Zhang N, Zhao Z, Li Q, Wu N, Fang P, Chang F, Wu Z.
Tian W, et al.
Mol Genet Genomics. 2022 Mar;297(2):387-396. doi: 10.1007/s00438-022-01853-x. Epub 2022 Feb 5.
Mol Genet Genomics. 2022.
PMID: 35122151
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[The multisystem deformities features of Klippel-Feil syndrome patients combined with congenital scoliosis].
Yin XJ, Li ZQ, Li GZ, Chen GL, Xu KX, Zhu YP, Zhang JG, Wu N.
Yin XJ, et al.
Zhonghua Yi Xue Za Zhi. 2024 Jan 2;104(1):16-21. doi: 10.3760/cma.j.cn112137-20231013-00731.
Zhonghua Yi Xue Za Zhi. 2024.
PMID: 38178763
Chinese.
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