Yorifuji T | Kyoto University
スポンサーリンク
概要
関連著者
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Ogata T
Tokyo Ohka Kogyo Co. Ltd. Kanagawa Jpn
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HASEGAWA T
Keio University
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Muroya K
Tokyo Dental College Ichikawa General Hospital
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Yorifuji T
Kyoto University
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Hasegawa T
Department Of Paediatrics Keio University School Of Medicine
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Ogata T
Tokyo Electric Power Company Hospital
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Sasaki R
Keio Univ. School Of Medicine Tokyo Jpn
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Horikawa R
National Center for Child Health and Development
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Ogata T
National Center for Child Health and Development
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ADACHI M
Kanagawa Children's Medical Center
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TACHIBANA K
Kanagawa Children's Medical Center
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Sato S
Saitama Metropolitan Hospital
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Kinoshita E
Nagasaki University School of Medicine
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Naiki Y
Division Of Endocrinology And Metabolism Adolescent Medicine National Center For Child Health And De
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Matsuo N
National Center for Child Health and Development
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Hanew K
Hanew Endocrine Clinic
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Kinoshita E
Nagasaki Univ. School Of Medicine Nagasaki Jpn
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Inamo Y
Asahikawa Medical College
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Nakagomi Y
Yamanashi University School Of Medicine
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Shinohara O
Tokai University
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Ogawa E
Tohoku University
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Minagawa M
Chiba University
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Igarashi N
Toyama Prefecture Central Hospital
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Nose O
Nose Clinic
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Ogawa M
Ogawa Clinic
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Aikawa T
Aikawa Station Clinic
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Hasegawa Y
Kiyose Children's Hospital
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Aizu K
Saitama Children's Medical Center
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Nishi Y
Hiroshima Red-cross Hospital
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Horikawa R
Division Of Endocrinology And Metabolism Adolescent Medicine National Center For Child Health And De
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Kamimaki T
Shimuzu Municipal Hospital
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Inamo Y
Nippon University Hikarigaoka Hospital
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Ogata T
Department Of Endocrinology And Metabolism National Research Institute For Child Health And Developm
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Aizu K
Saitama Children's Medical Center
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Tachibana K
Kanagawa Children's Medical Center
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Horikawa R
Division Of Adolescent Medicine And Division Of Endocrinology & Metabolism
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Adachi M
Kanagawa Children's Medical Center
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Hasegawa Y
Tokyo Metropolitan Kiyose Children's Hospital
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Matsuo N
Department Of Paediatrics Keio University School Of Medicine
著作論文
- 29 TURNER SYNDROME AND XP DELETIONS : CLINICAL AND MOLECULAR STUDIES IN 47 PATIENTS
- 36 CONGENITAL ADRENAL HYPOPLASIA AND MENTAL RETARDATION : IMPORTNACE OF THE IL1RAPL GENE ANALYSIS