Shirakawa T. | Pediatric Dentistry, Hokkaido University Graduate School of Dental Medicine
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概要
- SHIRAKAWA T.の詳細を見る
- 同名の論文著者
- Pediatric Dentistry, Hokkaido University Graduate School of Dental Medicineの論文著者
関連著者
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Ariga T.
Department Of Pediatrics Hokkaido University Graduate School Of Medicine
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SAKIYAMA Y.
Department of Human Gene Therapy, Hokkaido University Graduate School of Medicine
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Kida M.
Research Group of Human Gene Therapy, Hokkaido University Graduate School of Medicine
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Ariga T.
Research Group of Human Gene Therapy, Hokkaido University Graduate School of Medicine
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Shirakawa T.
Pediatric Dentistry, Hokkaido University Graduate School of Dental Medicine
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Sakiyama Y.
Research Group of Human Gene Therapy, Hokkaido University Graduate School of Medicine
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Sakiyama Y.
Department Of Human Gene Therapy Hokkaido University Graduate School Of Medicine
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Sakiyama Y.
Research Group Of Human Gene Therapy Hokkaido University Graduate School Of Medicine
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Shirakawa T.
Pediatric Dentistry Hokkaido University Graduate School Of Dental Medicine
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Oguchi H.
Shimadzu Analytical & Measuring Center Inc.
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Kida M.
Department Of Pediatrics Hokkaido University Graduate School Of Medicine
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Ariga T.
Research Group Of Human Gene Therapy Hokkaido University Graduate School Of Medicine
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Oguchi H.
Pediatric Dentistry, Hokkaido University Graduate School of Dental Medicine
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TAKABAYASHI S.
Pediatric Dentistry Poplar Clinic
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SHIRAKAWA T.
Pedicatric Dentistry, Hokkaido University Graduate School of Dental Medicine
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OGUCHI H.
Pedicatric Dentistry, Hokkaido University Graduate School of Dental Medicine
著作論文
- The first report of a novel mutation in the amelogenin gene in a Japanese family affected with X-linked amelogenesis imperfecta (Oral Session)(Japanese Teratology Society 43rd Annual Meeting)
- Identification of a novel mutation in the enamelin gene in a Japanese family affected with autosomal dominant amelogenesis imperfecta(Oral Session)(Japanese Teratology Society 43rd Annual Meeting)
- Autosomal-dominant Hypoplastic Form of Amelogenesis Imperfecta Caused by an Enamelin Gene Mutation at the Exon-Intron Boundary