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Issue Date | Title | Author(s) | Source | scopus | WOS | Fulltext/Archive link | |
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1 | 2017 | A limb-girdle myopathy phenotype of RUNX2 mutation in a patient with cleidocranial dysplasia: A case study and literature review | Hsueh S.-J.; NI-CHUNG LEE ; SHU-HUA YANG ; Lin H.-I.; CHIN-HSIEN LIN | BMC Neurology | 5 | 5 |