Muta Hiromi | The Division Of Molecular And Clinical Genetics The Department Of Molecular Genetics Medical Institu
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The Division Of Molecular And Clinical Genetics The Department Of Molecular Genetics Medical Institu | 論文
- Clinically Mild, Atypical, and Aged Craniofacial Syndrome is Diagnosed as Crouzon Syndrome by Identification of a Point Mutation in the Fibroblast Growth Factor Receptor 2 Gene (FGFR2)
- Gene Expression of Erythropoietin in Hepatocellular Carcinoma.