96 A ONE-MONTH-OLD FEMALE NEONATE CASE OF NONCLASSICAL STEROID 21-HYDROXYLASE DEFICIENCY DIAGNOSED BY MOLECULAR ANALYSIS OF THE CYP21 GENE.
スポンサーリンク
概要
著者
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Yorifuji T
Department Of Baioscience And Biotechnology Shinshu University
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Yorifuji T
Department Of Pediatrics Kyoto University School Of Medicine
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Ikuno N
Department of Pediatrics Hyogo Prefectural Amagasaki Hospital
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Usui T
Clinical Research Institute Center for Endocrine and Metabolic Disease Kyoto National Hospital
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Honma K
Department of Laboratory Medicine Keio University School of Medicine
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Honma K
Department Of Clinical Laboratories Keio University School Of Medicine
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