A Male Patient Presenting with Major Clinical Symptoms of Glucocorticoid Deficiency and Skeletal Dysplasia, showing a Steroid Pattern Compatible with 17α-Hydroxylase/17m,20-Lyase Deficiency, but without Obvious CYP17 Gene Mutations
スポンサーリンク
概要
著者
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NISHIMURA GEN
Department of Radiology, Tokyo Metropolitan Children's Hospital
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Adachi Masanori
Department of Dental Materials Science, Division of Oral Functional Science and Rehabilitation, Asah
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ASAKURA YUMI
Department of Endocrinology & Metabolism, Clinical Research Institute, Kanagawa Children's Medical C
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TACHIBANA KATSUHIKO
Department of Endocrinology and Metabolism, Kanagawa Children's Medical Center
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Tachibana Katsuhiko
Department Of Endocrinology And Metabolism Kanagawa Children's Medical Center
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Nishimura G
Department Of Radiology Dokkyo University School Of Medicine
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Nishimura Gen
Department Of Pediatric Radiology Tokyo Metropolitan Kiyose Children's Hospital
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SUWA Seizo
Department of Endocrinology and Metabolism, Kanagawa Children's Medical Center
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Adachi Masanori
神奈川県立こども医療センター 内科系専門医療部門内分泌代謝科
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Adachi Masanori
Department Of Endocrinology & Metabolism Clinical Research Institute Kanagawa Children's Me
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Suwa Seizo
Department Of Endocrinology And Metabolism Kanagawa Children's Medical Center
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ADACHI Masanori
Department of Dental Materials and Science, Division of Oral Functional Science and Rehabilitation, Asahi University School of Dentistry
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Asakura Yumi
Department of Endocrinology and Metabolism, Kanagawa Children's Medical Center
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NISHIMURA Gen
Department of Pediatric Imaging, Tokyo Metropolitan Children's Medical Center
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