Human Genome Epidemiology Literature Finder
Rare Diseases
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Query Trace: Legius Syndrome[original query] |
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SPRED1 mutations (Legius syndrome): another clinically useful genotype for dissecting the neurofibromatosis type 1 phenotype. Journal of medical genetics 2009 Jul 46 (7): 431-7. Spurlock G, Bennett E, Chuzhanova N, Thomas N, Jim H-Ping, Side L, Davies S, Haan E, Kerr B, Huson S M, Upadhyaya |
[Clinical and genetic analysis of three children with Legius syndrome due to variants of SPRED1 gene]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2024 8 41 (8): 941-946. Xi Wang, Yaodong Zhang, Mengmeng Du, Haihua Yang, Xiaojing Liu, Mengqin Wang, Jiajia Chen, Yongxing Chen, Haiyan W |
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