Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Osteogenesis Imperfecta and CRTAP[original query] |
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Next-generation sequencing of common osteogenesis imperfecta-related genes in clinical practice. Scientific reports 2016 6 28417. Árvai Kristóf, Horváth Péter, Balla Bernadett, Tobiás Bálint, Kató Karina, Kirschner Gyöngyi, Klujber Valéria, Lakatos Péter, Kósa János |
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 |
Genetic analysis, phenotype spectrum and functional study of rare osteogenesis imperfecta caused by CRTAP Variants. The Journal of clinical endocrinology and metabolism 2024 1 . Bingna Zhou, Peng Gao, Jing Hu, Xiaoyun Lin, Lei Sun, Qian Zhang, Yan Jiang, Ou Wang, Weibo Xia, Xiaoping Xing, Mei |
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- Page last updated:Apr 29, 2024
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