スポンサーリンク
Division of Genetic Diagnosis, Institute of Medical Science, University of Tokyo | 論文
- Loci on murine chromosomes 7 and 13 that modify the phenotype of the NOA mouse, an animal model of atopic dermatitis
- Characterization of six base pair deletion in the putative HNF 1-binding site of human PXR promoter
- Current Knowledge on the Pathophysiology of Fanconi Anemia: From Genes to Phenotypes
- Linkage and association analyses of the osteoprotegerin gene locus with human osteoporosis