Further delineation of 9q22 deletion syndrome associated with basal cell nevus (Gorlin) syndrome : Report of two cases and review of the literature
スポンサーリンク
概要
- 論文の詳細を見る
- 2009-03-01
著者
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KUROSAWA Kenji
Division of Medical Genetics, Kanagawa Children's Medical Center
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Tanaka Yukichi
Division Of Pathology Kanagawa Children's Medical Center
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ITO Susumu
Division of Neurosurgery, Kanagawa Children's Medical Center
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Masuno Mitsuo
Division Of Medical Genetics Clinical Research Institute Kanagawa Children's Medical Center
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Kurosawa Kenji
Division Of Medical Genetics Kanagawa Children's Medical Center
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YAMAMOTO Kayono
Department of Genetic Counseling, Graduate School of Humanities and Sciences, Ochanomizu University
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YOSHIHASHI Hiroshi
Division of Medical Genetics, Kanagawa Children's Medical Center
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FURUYA Noritaka
Division of Medical Genetics, Kanagawa Children's Medical Center
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ADACHI Masanori
Division of Endocrinology and Metabolism, Kanagawa Children's Medical Center
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CHIYO Hideaki
Department of Genetic Counseling, Graduate School of Humanities and Sciences, Ochanomizu University
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Yoshihashi Hiroshi
Division Of Medical Genetics Kanagawa Children's Medical Center
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Adachi Masanori
Division Of Endocrinology And Metabolism Kanagawa Children's Medical Center
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Chiyo Hideaki
Department Of Genetic Counseling Graduate School Of Humanities And Sciences Ochanomizu University
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Furuya Noritaka
Division Of Medical Genetics Kanagawa Children's Medical Center
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Yamamoto Kayono
Department Of Genetic Counseling Graduate School Of Humanities And Sciences Ochanomizu University
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Kurosawa Kenji
Division Of Genetics Clinical Research Institute Kanagawa Children's Medical Center
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Masuno Mitsuo
Division Of Medical Genetics Kanagawa Children's Medical Center
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Ito Susumu
Division Of Neurosurgery Kanagawa Children's Medical Center
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Furuya Noritaka
Division Of Genetics Kanagawa Children's Medical Center
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Masuno Mitsuo
Division Of Cardiology Tokyo Metropolitan Children's Medical Center
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