Sugimoto Takuya | Department of Complexity Science and Engineering, University of Tokyo
スポンサーリンク
概要
関連著者
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Sugimoto Takuya
Department of Complexity Science and Engineering, University of Tokyo
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Shiina Masaaki
Department Of Biochemistry Yokohama City University Graduate School Of Medicine
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Mizokawa Takashi
Department Of Complexity Science And Engineering And Department Of Physics University Of Tokyo
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Miyake Noriko
Department Of Biochemistry And Molecular Biology And Division Of Gene Therapy Research Center For Ad
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Ikegawa Shiro
Laboratory For Bone And Joint Disease Snp Research Center Riken Institute Of Medical Science Univers
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Minami Satoshi
Department Of Internal Medicine 2 Sinshu University Medical School
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Ohashi Hirofumi
Division Of Medical Genetics Saitama Children's Medical Center
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Nakashima Mitsuko
Department Of Human Genetics Nagasaki University Graduate School Of Biomedical Sciences
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Iida Aritoshi
Laboratory For Bone And Joint Diseases Center For Genomic Medicine Riken
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Matsumoto Naomichi
Department Of Cardiology Fukuoka University Hospital School Of Medicine
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Saitsu Hirotomo
Department Of Anatomy And Developmental Biology Graduate School Of Medicine Kyoto University
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Tsurusaki Yoshinori
Department Of Human Genetics Yokohama City University Graduate School Of Medicine
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Ogata Kazuhiro
Department Of Biochemistry Yokohama City University Graduate School Of Medicine
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OKAMOTO Nobuhiko
Department of Medical Genetics, Osaka Medical Center and Research Institute for Maternal and Child Health
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Mizokawa Takashi
Department of Complexity Science and Engineering, University of Tokyo:Department of physics, University of Tokyo
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Ootsuki Daiki
Department of physics, University of Tokyo
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NISHIMURA Gen
Department of Pediatric Imaging, Tokyo Metropolitan Children's Medical Center
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WATANABE Shigehiko
Division of Medical Genetics, Saitama Children's Medical Center
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IIDA Aritoshi
Laboratory for Bone and Joint Diseases, Center for Genomic Medicine
著作論文
- 18aGB-8 Unrestricted Hartree-Fock study on orbital-disordered states in Ca_Sr_xRuO_4
- Exome sequencing identifies a novel INPPL1 mutation in opsismodysplasia