L1CAM mutation in a Japanese family with x-linked hydrocephalus: a study for genetic counseling
スポンサーリンク
概要
- 論文の詳細を見る
- 1997-12-01
著者
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MAKITA Yoshio
Department of Pediatrics, Asahikawa Medical Collage
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TAKAHASHI Satoru
Department of Experimental Pathology and Tumor Biology, Nagoya City University Graduate School of Me
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Makita Yoshio
Department Of Pediatrics Asahikawa Medical College
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OKAMOTO Nobuhiko
Department of Planning and Research, Osaka Medical Center and Research Institute for Maternal and Ch
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OKI JUNICHI
Department of Pediatrics, Asahikawa Kosei Hospital
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Takahashi Satoru
Department Of Pediatrics Asahikawa Medical College
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Oki Junichi
Department Of Pediatrics Asahikawa Medical College
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Oki Junichi
Department Of Pediatrics Asahikawa Kosei Hospital
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MIYAMOTO Akie
Department of Pediatrics, Asahikawa Medical College
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Miyamoto Akie
Department Of Pediatrics Asahikawa Medical College
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Okamoto Nobuhiko
Department Of Planning And Research Osaka Medical Center And Research Institute For Maternal And Chi
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Okamoto Nobuhiko
Department Of Planning And Research Osaka Medical Center And Research Instiute For Maternal And Chil
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Takahashi Satoru
Department Of Anatomy And Embryology Biomolecular And Integrated Medical Sciences Graduate School Of
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Okamoto Nobuhiko
Department Of Molecular Cytogenetics Medical Research Institute And School Of Biomedical Science Tokyo Medical And Dental University
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Miyamoto Akie
Department Of Dermatology Faculty Of Medicine University Of Tokyo
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TAKAHASHI Satoru
Department of Pediatrics, Asahikawa Medical College
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OKAMOTO Nobuhiko
Department of Medical Genetics, Osaka Medical Center and Research Institute for Maternal and Child Health
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Miyamoto A
Department of Pediatrics, Asahikawa Medical College
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