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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Nov 10, 2024. (Total: 233377Documents)
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Records 1 - 2 (of 2 Records)

Query Trace: Osteogenesis Imperfecta and PLOD2[original query]
Novel Mutations in PLOD2 Cause Rare Bruck Syndrome.
Calcified tissue international 2017 11 102 (3): 296-309.
Lv Fang, Xu Xiaojie, Song Yuwen, Li Lujiao, Asan , Wang Jian, Yang Huanming, Wang Ou, Jiang Yan, Xia Weibo, Xing Xiaoping, Li M
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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