スポンサーリンク
Department of Developmental Medicine (Pediatrics), D-5 Osaka University Graduate School of Medicine | 論文
- Novel mutation of gene coding for glial fibrillary acidic protein in a Japanese patient with Alexander disease
- Cow's milk allergy presenting Hirschsprung's disease-mimicking symptoms
- Mutation analysis of Japanese patient with fucosidosis
- Mutational analysis of MECP2 in Japanese patients with atypical Rett syndrome
- Mutation analysis of two Japanese patients with Fanconi-Bickel syndrome
- Development of a New Synthetic Method for L-Tetrahydrofuranylglycine and Its Application for Substrate-based HIV-1 Protease Inhibitors
- ALLELE FREQUENCIES OF INTRAGENIC, AND 5' AND 3' MARKERS OF THE DYSTROPHIN GENE IN JAPANESE FAMILIES AFFLICTED WITH DUCHENNE OR BECKER MUSCULAR DYSTROPHY
- A case of chronic infantile type of fucosidosis : clinical and magnetic resonance in image findings