Ohashi H. | Division Of Medical Genetics Saitama Children's Medical Center
スポンサーリンク
概要
関連著者
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Ohashi H.
Division of Cardiology Department of Internal Medicine, Prefectural Gifu Hospital, Department of Int
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Muto R.
Department Of Pediatrics Tokyo Womens Medical University
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Ohashi H.
Division Of Medical Genetics Saitama Children's Medical Center
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Osawa M.
Department of Pediatrics, Tokyo Womens Medical University
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KOSHO T.
Division of Medical Genetics, Saitama Children's Medical Center
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Kosho T.
Division Of Medical Genetics Saitama Children's Medical Center
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NAKAMURA K.
Department of Applied Chemistry, The University of Tokyo
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YAMAGUCHI S.
Division of Environmental Science, The Graduate School of Scienc and Technology, Kobe University
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Nagaki S.
Department Of Pediatrics Tokyo Womens Medical University
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Yokoya S.
Department Of Pediatrics Toranomon Hospital
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Ogunoi M.
Department of Pediatrics, Tokyo Womens Medical University
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Oguni H.
Department of Pediatrics, Tokyo Womens Medical University
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MUTO R.
Division of Medical Genetics, Saitama Children's Medical Center
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MANABE N.
Department of Orthopedic Surgery, University of Tokyo
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MOCHIZUKI H.
Division of Endocrinology and Metabolism, Saitama Children's Medical Center
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NISHIDA T.
Department of Clinical Laboratory, Saitama Children's Medical Center
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IKEGAWA S.
Laboratory for Bone and Joint Diseases, SNP Research Center, RIKEN
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NISHIMURA G.
Department of Radiology, Nasuchou Hospital
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KODA N.
Department of Endocrinology & Metabolism, Saitama Children's Medical Center
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KISHIMOTO H.
Department of Pathology, Saitama Children's Medical Unviersity
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Ogunoi M.
Department Of Pediatrics Tokyo Womens Medical University
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Oguni H.
Department Of Pediatrics Tokyo Womens Medical University
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Ikegawa S.
Laboratory For Bone And Joint Diseases Riken Snp Research Center
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Ikegawa S.
Laboratory For Bone And Joint Diseases Snp Research Center Riken:laboratory For Genome Medicine Ims
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Manabe N.
Department Of Orthopedic Surgery University Of Tokyo
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Koda N.
Department Of Endocrinology & Metabolism Saitama Children's Medical Center
著作論文
- Thirty-three year study of epileptic patients with chromosomal abnormalities
- B-6 Analysis of FGFR3 mutation in achondroplasia-group bone dysplasia.
- B-2 A Case of Moore-Federman syndrome.