PTPN11, SOS1, KRAS, and RAF1 gene analysis, and genotype-phenotype correlation in Korean patients with Noonan syndrome
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概要
- 論文の詳細を見る
- Springer Japanの論文
- 2008-11-01
著者
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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
韓国
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Yoo Han-wook
Medical Genetics Clinic And Laboratory
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Yoo Han-wook
Department Of Pediatrics Asan Medical Center University Of Ulsan College Of Medicine
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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 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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KIM Jae-Min
Genome Research Center for Birth defects and Genetic Diseases, Asan Medical Center, University of Ul
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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
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 Children's Hospital University Of Ulsan College Of
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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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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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Yoo Han-wook
Department Of Pediatrics Asan Medical Center
関連論文
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- Feasibility of gene therapy in Gaucher disease using an adeno-associated virus vector
- Identification and functional analysis of cystathionine beta-synthase gene mutations in patients with homocystinuria
- 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
- Molecular genetic and proteomic analysis in Korean patients with Wilson disease
- Predictive factors for organic central precocious puberty and utility of simplified gonadotropin-releasing hormone tests
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