Matsuo M | Department Of Clinical Evaluation Of Pediatrics Kobe University Graduate School Of Medicine
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概要
- 同名の論文著者
- Department Of Clinical Evaluation Of Pediatrics Kobe University Graduate School Of Medicineの論文著者
関連著者
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Matsuo M
Department Of Clinical Evaluation Of Pediatrics Kobe University Graduate School Of Medicine
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Matsuo M
Department Of Electrical And Electronic Engineering Faculty Of Engineering Ibaraki University:(prese
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Nakamura H
Department Of Analytical Chemistry Hoshi University
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Takeshima Y
Department Of Biology Faculty Of Science Kumamoto University
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Takeshima Y
Department Of Pediatrics Kobe University Graduate School Of Medicine
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Takeshima Y
Department of Pediatrics, Kobe University Graduate School of Medicine
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Yagi M
Department Of Astronomy Kyoto University
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Ishibashi K
Department Of Applied Physics And Dimes Delft University Of Technology:the Institute Of Physical And
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Adachi K
Department Of Electrical And Information Engineering Faculty Of Engineering Yamagata University
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Takeuchi K
Department Of Anatomy Gunma University School Of Medicine
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Nishio H
Department Of Genetic Epidemiology Kobe University Graduate School Of Medicine
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Kitoh Y
Department Of Pediatrics Kobe University School Of Medicine
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Yamamoto T
Department Of Anatomy And Developmental Neurobiology Kobe University Graduate School Of Medicine
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Goji K
Department Of Endocrinology And Metabolism Kobe Children's Hospital
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Nishio H
Division of Pubic Health, Kobe University Graduate School of Medicine
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Deguchi M
Division Of Molecular Medicine Kobe University Graduate School Of Medicine
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Yagi M
Division of Molecular Medicine, Kobe University Graduate School of Medicine
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Goji K
Departmcnt Of Endocrinology And Metabolism Kobe Children's Hospital
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Kurosaka M
Department Of Orthopedic Surgery Kobe University Graduate School Of Medicine
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Nishio H
Department Of Epidemiology Kobe University Graduate School Of Medicine
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Goji K
Departmcnt of Endocrinology and Metabolism , Kobe Children's Hospital
著作論文
- Amplification of selected exons by polymerase chain reaction enables determination of the translational reading frame of dystrophin mRNA resulting from deletion mutations.
- 185 A 3-YEARS-OLD GIRL WITH AUTOIMMUNE HYPO-THYROIDISM CARRYING A MISSENSE MUTATION OF THYROGLOBULIN(TG) GENE
- 209 A CASE OF PRIMARY HYPOTHYROIDISM WITH REVERSION OF GONADOTROPIN INDEPENDENT TO GONADOTROPIN DEPENDENT PRECOCIOUS PUBERTY
- 240 A CASE OF PSEUDOHYPOPARATHYROIDISM WITH SUBCTANEOUS METAPLASTIC BONE FORMATION