Congenital hyperinsulinism in an infant with paternal uniparental disomy on chromosome 11p15 : Few clinical features suggestive of Beckwith-Wiedemann syndrome
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概要
- 論文の詳細を見る
- 2013-04-01
著者
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Higashimoto Ken
Division Of Molecular Genetics And Epigenetics Department Of Biomolecular Sciences Faculty Of Medici
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Soejima Hidenobu
Division Of Molecular Genetics And Epigenetics Department Of Biomolecular Sciences Faculty Of Medici
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Adachi Hiroyuki
Department Of Biotechnology Graduate School Of Agricultural And Life Sciences University Of Tokyo
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Ito Tomoo
Department Of Diagnostic Pathology Kobe University Graduate School Of Medicine
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Masue Michiya
Department Of Pediatrics Shimane Medical University
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Noguchi Atsuko
Department Of Pediatrics Akita University Graduate School Of Medicine
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Tamura Hiroaki
Department Of Applied Chemistry Waseda University
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Nishibori Hironori
Department Of Radiology Kizawa Memorial Hospital
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Tsuchida Satoko
Department Of Pediatrics Akita University Graduate School Of Medicine
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Takahashi Tsutomu
Department Of Dermatology Kobe University School Of Medicine
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Takahashi Ikuko
Department of Neurology, Hokkaido University Graduate School of Medicine
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Takahashi Ikuko
Department of Pediatrics, Akita University Graduate School of Medicine
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Arai Hirokazu
Department of Human Sciences, Osaka University of Human Sciences
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ITO Tomoo
Department of Pediatrics, Akita University Graduate School of Medicine
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