Ogata Tsutomu | Department Of Molecular Endocrinology National Research Institute For Child Health And Development
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概要
- 同名の論文著者
- Department Of Molecular Endocrinology National Research Institute For Child Health And Developmentの論文著者
関連著者
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Ogata Tsutomu
Department Of Endocrinology And Metabolism National Research Institute For Child Health And Developm
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Ogata Tsutomu
Department Of Molecular Endocrinology National Research Institute For Child Health And Development
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Fukami Maki
Department Of Endocrinology And Metabolism National Research Institute For Child Health And Developm
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Ogata Tsutomu
Ntt
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Fukami Maki
Department Of Endocrinology And Metabolism National Research Institute For Child Health And Developm
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Fukami Maki
Department Of Molecular Endocrinology National Research Institute For Child Health And Development
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Ogata T
Department Of Endocrinology And Metabolism National Research Institute For Child Health And Developm
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Muroya Koji
Department Of Endocrinology And Metabolism Kanagawa Children's Medical Center
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ISO Manami
Department of Molecular Endocrinology, National Research Institute for Child Health and Development
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Iso Manami
Department Of Molecular Endocrinology National Research Institute For Child Health And Development
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Yokoi Hisashi
Department Of Cardiology Juntendo University School Of Medicin
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Horikawa Reiko
Division Of Endocrinology And Metabolism National Center For Child Health And Development
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Kato Fumiko
Department Of Endocrinology And Metabolism National Research Institute For Child Health And Developm
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Matsubara Keiko
Department Of Cardiology Rakusai Newtown Hospital
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Dateki Sumito
Department Of Endocrinology And Metabolism National Research Institute For Child Health And Developm
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Sasaki Goro
Department Of Electrical Engineering Kyoto University
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Miyake Tetsuo
Department Of Agricultural Chemistry The University Of Tokyo
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Nagai Toshiro
Department Of Pediatrics Dokkyo Medical University Koshigaya Hospital
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Murakami Nobuyuki
Department Of Anatomy And Structural Biology University Of Otago
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Fujita Keinosuke
Department Of Pediatrics Children's Medical Center Osaka City General Hospital
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Mochizuki Takahiro
Department Of General Thoracic Surgery Seirei Hamamatsu General Hospital
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Nakagomi Yoshiko
Department Of Pediatrics Yamanashi Medical University
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ITAKURA Mitsuo
Institute for Genome Research, University of Tokushima
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Kikuchi Nobuyuki
Department Of Pediatrics Yokohama City University Medical Center
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Suzuki Yoshimi
Department Of Nutritional Science Tokyo University Of Agriculture
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Moriuchi Hiroyuki
Department Of Molecular Microbiology And Immunology Nagasaki University Graduate School Of Biomedica
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Tanaka Yoko
Department Of Applied Biological Chemistry Graduate School Of Agricultural And Life Sciences The Uni
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Miyake Tetsuo
Department Of Molecular Endocrinology National Research Institute For Child Health And Development
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TSUBOUCHI Koji
Department of Pediatrics, Mino Municipal Hospital
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Tsubouchi Koji
Department Of Pediatrics Mino Municipal Hospital
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Mochizuki Takahiro
Department Of Pediatrics Children's Medical Center Osaka City General Hospital
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Yokoi Hisashi
Department Of Internal Medicine Japanese Red Cross Nagoya First Hospital
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Kikuchi Nobuyuki
Department Of Pediatrics Yokohama City University Hospital
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Nakagomi Yoshiko
Department Of Pediatrics Yamanashi University Hospital
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Fujita Keinosuke
Department Of Pediatrics And Pediatric Emergency Medicine Osaka City General Hospital
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Itakura Mitsuo
Institute For Genome Research Tokushima University
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Tanaka Yoko
Department Of Pediatrics Tokyo Dental College Ichikawa General Hospital
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Suzuki Yoshimi
Department Of Pediatrics Atsumi Hospital
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Nagai Toshiro
Department Of Medical Genetics Tohoku University School Of Medicine
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Sasaki Goro
Department Of Pediatrics Tokyo Dental College Ichikawa General Hospital
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FUJITA KEINOSUKE
Department of Pediatrics, Children's Medical Center, Osaka City General Hospital
著作論文
- GATA3 abnormalities in six patients with HDR syndrome
- Diabetes Mellitus in a Japanese Girl with HDR Syndrome and GATA3 Mutation
- Identification of chromosome 15q26 terminal deletion with telomere sequences and its bearing on genotype-phenotype analysis
- Maternal age effect on the development of Prader-Willi syndrome resulting from upd(15)mat through meiosis 1 errors