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Department Of Molecular Medicine Osaka Medical Center And Research Institute For Maternal And Child | 論文
- A NOVEL MUTATION IN L1CAM GENE IN A JAPANESE PATIENT WITH X-LINKED HYDROCEPHALUS
- A clinical and molecular study of a patient with Simpson-Golabi-Behmel syndrome
- Effect of Exogenous Decorin on Cell Morphology and Attachment of Decorin-Deficient Fibroblasts^1
- Aberrant Expressions of Decorin and Biglycan Genes in the Carbohydrate-Deficient Glycoprotein Syndrome
- Hemoglobin Tokyo II [α89 (FG1) His→Asn] : A New Hemoglobin Variant Characterized by Endoproteinase Asp-N Digestion and Collision-Induced Dissociation
- Advanced analytical methods for hemoglobin variants