Huang Lijun | Department Of Biochemistry Hainan Medical College
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概要
関連著者
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Huang Lijun
Department Of Biochemistry Hainan Medical College
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Ma Qiuling
Department Of Biochemistry Hainan Medical College
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Wang Wei
Department Of Biochemistry Hainan Medical College
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Wang Xiaoying
Department Of Biochemistry Kobe University School Of Medicine
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Yang Zhigang
Department Of Materials Science And Engineering Tsinghua University
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Han Yong
Department Of Endocrinology Provincial Hospital Affiliated To Shandong University
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Wang Wei
Department Of Biology Graduate School Chinese Academy Of Sciences Beijing
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Du Guankui
Department Of Biochemistry Hainan Medical College
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Xiao Man
Department Of Biochemistry Hainan Medical College
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Li Gang
Department Of Biochemistry And Molecular Biology Peking University Health Science Center
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Cai Wangwei
Department Of Biochemistry Hainan Medical College
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HUANG Lijun
Department of Biochemistry, Hainan Medical College
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XIAO Deqian
Department of Biochemistry, Hainan Medical College
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CHEN Xiaodan
The Clinical Laboratory, Affiliated Hospital of Hainan Medical College
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ZHOU Keyuan
Department of Biochemistry, Guangdong Medical College
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HAO Xinbao
Department of Hematology, Affiliated Hospital of Hainan Medical College
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Chen Xiaodan
The Clinical Laboratory Affiliated Hospital Of Hainan Medical College
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Hao Xinbao
Department Of Hematology Affiliated Hospital Of Hainan Medical College
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Yang Zhigang
Department Of Hematology Affiliated Hospital Of Guangdong Medical College
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Zhou Keyuan
Department Of Biochemistry Guangdong Medical College
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Xiao Deqian
Department Of Biochemistry Hainan Medical College
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WANG Xiaoying
Department of Biochemistry, Hainan Medical College
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Wang Wei
Department of Anesthesiology, China-Japan Friendship Hospital, the Chinese Ministry of Health, Beijing, China
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Lu Qiang
Department of Thoracic Surgery, Tangdu Hospital, Fourth Military Medical University, Xian, China
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Yan Xiaolong
Department of Thoracic Surgery, Tangdu Hospital, Fourth Military Medical University, Xian, China
著作論文
- Homozygous intronic mutation leading to inefficient transcription combined with a novel frameshift mutation in F13A1 gene causes F13 deficiency
- Homozygous intronic mutation leading to inefficient transcription combined with a novel frameshift mutation in F13A1 gene causes FXIII deficiency
- A 5-year-old Boy with a Large Hereditary Multiple Exostoses Lump Grown into Thoracic Cavity