Human Genome Epidemiology Literature Finder
Rare Diseases
Records 1 - 2 (of 2 Records) |
Query Trace: Bruck Syndrome 2[original query] |
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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 |
Diagnostic strategies and genotype-phenotype correlation in a large Indian cohort of osteogenesis imperfecta. Bone 2018 3 110 368-377. Mrosk Julia, Bhavani Gandham SriLakshmi, Shah Hitesh, Hecht Jochen, Krüger Ulrike, Shukla Anju, Kornak Uwe, Girisha Katta Moh |
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- Page last updated:May 13, 2024
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