Yang Chi-fan | 台湾
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概要
関連著者
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Yang Chi-fan
台湾
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Yang Chi-fan
Department Of Medical Genetics China Medical College Hospital
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Lee Cheng-chun
Department Of Neurology China Medical College Hospital
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TSAI Chang-Hai
Department of Medical Research, China Medical College Hospital
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Wu Jer-yuran
Department Of Medical Research China Medical College Hospital
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Wu Jer-yuarn
Department Of Medical Genetics China Medical College Hospital
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Lee Cheng-chun
Department Of Medical Research China Medical College Hospital
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Tsai Fuu-jen
Department Of Pediatrics China Medical College Hospital
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Tsai Chang-hai
Taichung Healthcare And Management University
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李 正淳
中国医薬学院附設医院
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Tsai Chang-hai
台湾
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児玉 浩子
東京都立八王子小児病院 小児内科
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TSAI Fuu-Jen
Department of Medical Research, China Medical College Hospital
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Wu Jer-Yuarn
Department of Pediatrics and Medical Genetics, China Medical College Hospital
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Tsai Chang-hai
Department Of Medical Research China Medical College Hospital
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Tsai Fuu-jen
Department Of Medical Research China Medical College Hospital
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ABE Toshiaki
Department of Neurosurgery, The Jikei University School of Medicine
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村田 佳子
帝京大・医・小児科
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村田 佳子
帝京大学 小児科
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児玉 浩子
帝京大学小児科
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KODAMA Hiroko
Department of Community Health and Clinical Epidemiology, St. Mary's College
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Kodama Hiroko
帝京大学 医学部医学科
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Abe Toshiaki
Department Of Neurosurgery Jikei University School Of Medicine
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村田 佳子
帝京大学小児科
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Kodama Hiroko
Department Of Pediatrics School Of Medicine Teikyo University
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Kodama H
Teikyo Univ. School Of Medicine Tokyo Jpn
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Abe Toshiaki
Department Of Pediatrics Teikyo University Hospital
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Kodama Hiroko
Department Of Community Health And Clinical Epidemiology St. Mary's College
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WU Jer-Yuarn
China Medical College Hospital
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TSAI Fuu-Jen
China Medical College Hospital
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YANG Chi-Fan
China Medical College Hospital
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TSAI Chang-Hai
China Medical College Hospital
著作論文
- Molecular analysis of Wilson disease in Taiwan: identification of one novel mutation and evidence of haplotype-mutation association
- Mutation analysis of Crouzon syndrome and identification of one novel mutation in Taiwanese patients
- 台湾人 Wilson 病患者のATP7B遺伝子異常とハプロタイプ