Kim Gu-hwan | Medical Genetics Clinic And Laboratory
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概要
関連著者
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Yoo Han-wook
韓国
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Yoo Han-wook
Medical Genetics Clinic And Laboratory
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Kim Gu-hwan
Medical Genetics Clinic And Laboratory
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Kim Gu-hwan
Medical Genetics Clinic And Laboratory Asan Medical Center University Of Ulsan College Of Medicine
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Yoo Han-wook
Department Of Pediatrics Asan Medical Center Children's Hospital University Of Ulsan College Of
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Kim Gu-hwan
Asan Medical Center University Of Ulsan College Of Medicine
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Yoo Han-wook
Department Of Pediatrics Asan Medical Center
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Choi Jin-ho
Department Of Computer Engineering Pusan University Of Foreign Studies
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Choi Jin-ho
Department Of Pediatrics Chungnam National University Hospital College Of Medicine Chungnam National
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Kim Gu-hwan
Medical Genetics Center Asan Medical Center Children's Hospital University Of Ulsan College Of
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Yoo Han-wook
Department Of Pediatrics Asan Medical Center University Of Ulsan College Of Medicine
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Lee Beom
Department Of Gastroenterology Korea University Guro Hospital
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Ko Jung
Genome Research Center For Birth Defects And Genetic Diseases Asan Medical Center Children's Hospital University Of Ulsan College Of Medicine
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Lee Beom
Department Of Pediatrics Asan Medical Center Children's Hospital University Of Ulsan College Of Medicine
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YOO Han-Wook
Department of Pediatrics, Medical Genetics Clinic and Laboratory, Asan Medical Center, University of
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Yoo Han-wook
Department Of Pediatrics Medical Genetics And Laboratory Asan Medical Center University Of Ulsan Col
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Ko Jung
Department Of Pediatrics Asan Medical Center University Of Ulsan College Of Medicine
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Kim Jae-min
Genome Research Center For Birth Defects And Genetic Diseases Asan Medical Center University Of Ulsa
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Ko Jung
Department Of Mathematics Kangnung National University
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Kim Gu-hwan
Genome Research Center For Birth Defects And Genetic Diseases Asan Medical Center Children's Hospital University Of Ulsan College Of Medicine
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Yang Song
Green Cross Reference Laboratory
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Kim Joo
Genome Research Center For Birth Defects And Genetic Diseases Asan Medical Center Children's Hospital University Of Ulsan College Of Medicine
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Kim Jae-min
Genome Research Center For Birth Defects And Genetic Diseases Asan Medical Center Children's Hospital University Of Ulsan College Of Medicine
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Choi Jin-Ho
Department of Emergency Medicine, Cardiac and Vascular Center, Cardiovascular Imaging Center, Samsun
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Park Sang-wook
Genome Research Center For Birth Defect & Genetic Disorders
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KIM Gu-Hwan
Department of Pediatrics, Medical Genetics Clinic & Laboratory Asan Medical Center, University of Ul
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KIM Kyung-Mo
Department of Pediatrics, Medical Genetics Clinic & Laboratory Asan Medical Center, University of Ul
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KIM Youngho
Genome Research Center for Birth Defect & Genetic Disorders
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YOO Han-Wook
Genome Research Center for Birth Defect & Genetic Disorders
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Yoo Han-wook
Medical Genetics Clinic & Laboratory Department Of Pediatrics Asan Medical Center University Of
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Yoon Hye-ran
Biomedical And Pharmaceutical Analysis Laboratory Department Of Analytical Chemistry School Of Pharm
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Kim Youngho
Genome Research Center For Birth Defect & Genetic Disorders
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Kim Kyung-mo
Department Of Pediatrics Medical Genetics Clinic & Laboratory Asan Medical Center University Of
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KIM Jae-Min
Genome Research Center for Birth defects and Genetic Diseases, Asan Medical Center, University of Ul
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KIM Gu-Hwan
Asan Medical Center, University of Ulsan College of Medicine
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Yoon Hye-ran
Biomedical & Pharmaceutical Analysis Lab College Of Pharmacy Duksung Women's University
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Lee Jin
Department Of Biology Inha University
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Cheon Chong
Department Of Pediatrics Genetic And Metabolic Clinic Children Hospital Pusan National University
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Jung Chang-woo
Department Of Pediatrics Asan Medical Center Children's Hospital University Of Ulsan College Of Medicine
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Lee Jin
Department Of Pediatrics Asan Medical Center Children's Hospital University Of Ulsan College Of Medicine
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Kang Duk-hee
Division Of Nephrology Department Of Internal Medicine Ewha Womans University School Of Medicine Ewha Medical Research Center
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HEO Sun
Genome Research Center for Birth Defects and Genetic Disorders, University of Ulsan College of Medicine, Asan Medical Center
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PARK Jung-Young
Genome Research Center for Birth Defects and Genetic Disorders, University of Ulsan College of Medicine, Asan Medical Center
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KIM Woo-Shik
Division of Cardiology, Department of Internal Medicine, School of Medicine, Kyung Hee University
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CHOE Kyung
Department of Cardiology, Wonju College of Medicine, Yonsei University
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KIM Won-Ho
Department of Cardiovascular Medicine, Medical School of Chonbuk National University
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YANG Song
Institute of Metabolism, Green Cross Reference Laboratory
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Heo Sun
Genome Research Center For Birth Defects And Genetic Disorders University Of Ulsan College Of Medicine Asan Medical Center
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Choe Kyung
Department Of Cardiology Wonju College Of Medicine Yonsei University
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Kim Woo-shik
Division Of Cardiology Department Of Internal Medicine School Of Medicine Kyung Hee University
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Park Jung-young
Genome Research Center For Birth Defects And Genetic Disorders University Of Ulsan College Of Medicine Asan Medical Center
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Kang Minji
Genome Research Center For Birth Defects And Genetic Diseases Asan Medical Center Children's Hospital University Of Ulsan College Of Medicine
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KIM Jon
Genome Research Center for Birth defects and Genetic Diseases, Asan Medical Center Children's Hospital, University of Ulsan College of Medicine
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Kim Won-ho
Department Of Cardiovascular Medicine Medical School Of Chonbuk National University
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Kim Jon
Genome Research Center For Birth Defects And Genetic Diseases Asan Medical Center Children's Hospital University Of Ulsan College Of Medicine
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LEE Jin
Department of Biochemistry, College of Medicine, Inje University
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Lee Jin
Department of Anatomy and Cell Biology, Collage of Medicine, Hanyang University
著作論文
- Mutation spectrum and polymorphisms in the human ATP7B gene and diverse phenotype of Korean patients with Wilson Disease
- PTPN11, SOS1, KRAS, and RAF1 gene analysis, and genotype-phenotype correlation in Korean patients with Noonan syndrome
- Genotypes and clinical features of Korean patients with methylmalonic aciduria and propionic aciduria
- Identification of novel mutations of the ATP7A gene and prenatal diagnosis of Menkes disease by mutation analysis
- Enzyme replacement therapy for Fabry disease in Korea
- Uneventful clinical courses of Korean patients with methylcrotonylglycinuria and their common mutations
- Mutations of the GLA gene in Korean patients with Fabry disease and frequency of the E66Q allele as a functional variant in Korean newborns
- Low prevalence of classical galactosemia in Korean population