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Department of Public Health, Kobe University Graduate School of Medicine | 論文
- Complementation Group Analysis of Four Chinese Xeroderma Pigmentosum Patients
- 良性家族性新生児痙攣を有する日本人一家系内の生殖細胞に生じたKCNQ2遺伝子変異(p. R213W)
- 日本人のSMN1遺伝子上にC117T多型を見出した
- Evaluation of mutation effects on UGT1A1 activity toward 17β-estradiol using liquid chromatography-tandem mass spectrometry
- Prenatal diagnosis of a Japanese family at risk for tay-sachs disease : application of a fluorescent competitive allele-specific polymerase chain reaction (pcr) method
- Screening for G71R mutation of the UGT1A1 gene in the Javanese-Indonesian and Malay-Malaysian populations
- ACE Gene Polymorphism in Children with Nephrotic Syndrome in the Indonesian Population
- Spectrum of Spontaneous Mutations in the Cyclic AMP Receptor Protein Gene on Chromosomal DNA of Escherichia coli
- Double fetus-in-fetu : A case report with three-dimensional computed tomography findings
- Recovery from Ultraviolet Light-Induced Depression of Ribosomal RNA Synthesis in Normal Human, Xeroderma Pigmentosum and Cockayne Syndrome Cells
- Recovery of RNA Synthesis Coupled with In Vitro Repair of UV Damage in Plasmid DNA
- Recovery from UV-induced initial depression of ribosomal RNA synthesis in normal and xeroderma piginentosum group A cells
- In Vitro Repair System using Human cell Extracts
- Spectrum of Spontaneous Mutation of E. Ccli Crp Gene
- Molecular genetic analysis and mutation screening of the vhl gene in a Japanese family with von hippel-lindau disease
- NAIP-Deletion Analysis in Malaysian Patients with Spinal Muscular Atrophy