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Department Of Cell And Developmental Biology School Of Dentistry Seoul National University | 論文
- Fam83h is Associated with Intracellular Vesicles and ADHCAI
- MMP20 Hemopexin Domain Mutation in Amelogenesis Imperfecta
- Candidate Gene Strategy Reveals ENAM Mutations
- A Novel Mutation in the DSPP Gene Associated with Dentinogenesis Imperfecta Type II
- Amelogenin p. M1T and p. W4S Mutations Underlying Hypoplastic X-linked Amelogenesis Imperfecta
- ENAM Mutations in Autosomal-dominant Amelogenesis Imperfecta
- DLX3 Mutation in a New Family and Its Phenotypic Variations
- Phenotypic Variation in Dentinogenesis Imperfecta/Dentin Dysplasia Linked to 4q21
- Novel WDR72 Mutation and Cytoplasmic Localization
- Novel MSX1 Frameshift Causes Autosomal-dominant Oligodontia