Yuasa Isao | Department Of Legal Medicine Tottori University School Of Medicine
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概要
関連著者
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Yuasa Isao
Department of Legal Medicine, Tottori University School of Medicine
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Yuasa Isao
Department Of Legal Medicine Tottori University School Of Medicine
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Yuasa Isao
Department Of Legal Medicine Faculty Of Medicine Tottori University
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KUWAJIMA Katsuko
Department of Pediatrics, Ibaraki Prefectural Handicapped Children's Center
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KONDO Ikuko
Department of Medical Genetics, Ehime University School of Medicine
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YASUDA Toshihiro
Division of Medical Genetics and Biochemistry, Faculty of Medical Sciences, University of Fukui
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Takeshita Haruo
Department Of Legal Medicine And Molecular Genetics Gunma University Graduate School Of Medicine
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NAKAJIMA Tamiko
Department of Legal Medicine and Molecular Genetics Gunma University, Graduate School of Medicine
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Shigemoto Kazuhiro
Department of Medical Genetics, Ehime University School of Medicine
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Tsuchio Yasukiro
Division Of Medical Genetics And Biochemistry Faculty Of Medical Sciences University Of Fukui
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Takeshita Haruo
Dep. Of Legal Medicine Shimane Univ. School Of Medicine
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Iida Reiko
Department Of Legal Medicine Fukui Medical University
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Kondo Ikuko
Department Of Hygiene Ehime University School Of Medicine
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Kishi Koichiro
Department Of Legal Medicine And Molecular Genetics Gunma University Graduate School Of Medicine
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Yasuda Toshihiro
Division Of Medical Genetics And Biochemistry Faculty Of Medical Sciences University Of Fukui
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IIDA Reiko
Division of Legal Medicine, Faculty of Medical Sciences, University of Fukui
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Shigemoto Kazuhiro
Department Of Anatomy And Embryology Ehime University School Of Medicine
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Nakajima Tamiko
Department Of Legal Medicine Gunma University Graduate School Of Medicine
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KOFLER Andrea
Institute of Anthropology and Human Genetics, University of Munich
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BRAUN Andreas
Institute of Anthropology and Human Genetics, University of Munich
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BICHLMAIER Regina
Institute of Anthropology and Human Genetics, University of Munich
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KAMMERER Stefan
Institute of Anthropology and Human Genetics, University of Munich
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CLEVE Hartwig
Institute of Anthropology and Human Genetics, University of Munich
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MIZUGISHI Kiyomi
Department of Pediatrics, Tokyo University School of Medicine
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YAMANAKA Keiko
Department of Pediatrics, Ibaraki Handicapped Children's Hospital
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UEKI Misuzu
Division of Medical Genetics and Biochemistry, Faculty of Medical Sciences, University of Fukui
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Kammerer Stefan
Institute Of Anthropology And Human Genetics University Of Munich
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Braun Andreas
Institute Of Anthropology And Human Genetics University Of Munich
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Cleve Hartwig
Institute Of Anthropology And Human Genetics University Of Munich
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Kofler Andrea
Institute Of Anthropology And Human Genetics University Of Munich
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Ueki Misuzu
Division Of Medical Genetics And Biochemistry Faculty Of Medical Sciences University Of Fukui
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Yamanaka Keiko
Department Of Pediatrics Ibaraki Handicapped Children's Hospital
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Yamanaka Keiko
Department Of Biology Faculty Of Science Ochanomizu University
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Bichlmaier Regina
Institute Of Anthropology And Human Genetics University Of Munich
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Shigemoto Kazuhiro
Department Of Hygiene Ehime University School Of Medicine
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Kominato Yoshihiko
Department Of Forensic Medicine Faculty Of Medicine Toyama Medical And Pharmaceutical University
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Mizugishi Kiyomi
Department Of Pediatrics Tokyo University School Of Medicine
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Kuwajima Katsuko
Department Of Pediatrics Ibaraki Handicapped Children's Hospital
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Yasuda Toshihiro
Division Of Medical Genetics And Biochemistry Faculty Of Medical Sciences Univerisity Of Fukui
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TSUKAHARA Tetsuya
Scientific Investigation Laboratory, Fukui Prefectural Police Headquarters
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Kagawa Yoshihiko
Division Of Cardiology Gunma Prefectural Cardiovascular Center
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Tsukahara Tetsuya
Scientific Investigation Laboratory Fukui Prefectural Police Headquarters
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Kominato Yoshihiko
Department Of Legal Medicine Graduate School Of Medicine Gunma University
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KUWAJIMA Katsuko
Department of Pediatrics, Ibaraki Handicapped Children's Hospital
著作論文
- A NOVEL SEQUENCE POLYMORPHISM IN EXON 8 OF THE HUMAN VITAMIN D-BINDING PROTEIN (GC) GENE IN AN AFRICAN POPULATION
- Missense mutations in the phosphomannomutase 2 gene of two Japanese siblings with carbohydrate-deficient glycoprotein syndrome type I
- A novel 56-bp variable tandem repeat polymorphism in the human deoxyribonuclease I gene and its population data