A Case of a Preterm Infant with 21-Hydroxylase Deficiency : Implications of the Biochemical Diagnosis with Urinary Pregnanetriolone by Gas Chromatography/Mass Spectrometry in Selected Ion Monitoring (GCMS-SIM)
スポンサーリンク
概要
著者
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OHKI Shigeru
Department of Neonatology Seirei-Hamamatsu Hospital
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HASEGAWA TOMONOBU
Department of Pediatrics, Keio University School of Medicine
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MIZUNO Haruo
Department of Pediatrics, Neonatology and Congenital Disorders, Nagoya City University Graduate Scho
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Mizuno Haruo
Department Of Biotechnology Graduate School Of Engineering Osaka University
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Ohki Shigeru
Department Of Pediatrics Seirei Hamamatsu Hospital
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Ohki Shigeru
Department Of Intensive Care And Second Department Of Surgery Gunma University Graduate School Of Me
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Homma Keiko
Department Of Laboratory Medicine Keio University School Of Medicine
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HAMAJIMA Takashi
Department of Pediatrics, Seirei Hamamatsu General Hospital
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Imamine Hiroki
Department of Pediatrics, Neonatology and Congenital Disorders, Nagoya City University Graduate Scho
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Imamine Hiroki
Department Of Pediatrics Neonatology And Congenital Disorders Nagoya City University Graduate School
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Hamajima Takashi
Department Of Pediatrics Seirei Hamamatsu Hospital : Department Of Endocrinology Aichi Children&apos
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Hamajima Takashi
Department Of Pediatrics Seirei Hamamatsu General Hospital
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Hasegawa Tomonobu
Department Of Pediatrics Keio University School Of Medicine
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Mizuno Haruo
Department Of Pediatrics Neonatology And Congenital Disorders Nagoya City University Graduate School
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Hamajima Takashi
Department Of Pediatric Endocrinology And Metabolism Aichi Children's Health And Medical Center
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