Showing results 1 to 2 of 2
Issue Date | Title | Journal Title |
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2009 | A novel PHEX mutation in a Korean patient with sporadic hypophosphatemic rickets. | ANNALS OF CLINICAL AND LABORATORY SCIENCE |
2009 | The First Korean Case of Camurati-Engelmann Disease (Progressive Diaphyseal Dysplasia) Confirmed by TGFB1 Gene Mutation Analysis | JOURNAL OF KOREAN MEDICAL SCIENCE |