Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Osteogenesis Imperfecta and SERPINH1[original query] |
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Novel compound heterozygous mutations in SERPINH1 cause rare autosomal recessive osteogenesis imperfecta type X. Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA 2018 3 29 (6): 1389-1396. Song Y, Zhao D, Xu X, Lv F, Li L, Jiang Y, Wang O, Xia W, Xing X, Li |
Osteogenesis imperfecta in Brazilian patients. Genetics and molecular biology 2019 8 42 (2): 344-350. Trancozo Maira, Moraes Marcos V D, Silva Dalila A, Soares Jéssica A M, Barbirato Clara, Almeida Márcio G, Santos Lígia R, Rebouças Maria R G O, Akel Akel N, Sipolatti Valentim, Nunes Vanda R R, Errera Flavia I V, Aguena Meire, Passos-Bueno Maria R, Paula Flavia |
Genotypic and Phenotypic Analysis in Chinese Cohort With Autosomal Recessive Osteogenesis Imperfecta. Frontiers in genetics 2020 10 11 984. Li Shan, Cao Yixuan, Wang Han, Li Lulu, Ren Xiuzhi, Mi Huan, Wang Yanzhou, Guan Yun, Zhao Feiyue, Mao Bin, Yang Tao, You Yi, Guan Xin, Yang Yujiao, Zhang Xue, Zhao Xiu |
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- Page last updated:Apr 29, 2024
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