Single nucleotide polymorphism in a commonly utilized LAMB3 primer sequence : Implications for mutation detection and haplotype analysis in junctional epidermolysis bullosa
スポンサーリンク
概要
- 論文の詳細を見る
- 2006-10-01
著者
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MCGRATH John
Genetic Skin Disease Group, St. John's Institute of Dermatology, Division of Genetics and Molecular
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Mcgrath John
Genetic Skin Disease Group And The Robin Eady National Diagnostic Epidermolysis Bullosa Research Lab
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Liu Lu
Genetic Skin Disease Group And The Robin Eady National Diagnostic Epidermolysis Bullosa Research Lab
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CHOY Yew
Genetics and Metabolism Unit, Paediatric Institute, Kuala Lumpur Hospital
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WESSAGOWIT Vesarat
Genetic Skin Disease Group and The Robin Eady National Diagnostic Epidermolysis Bullosa Research Lab
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OZOEMENA Linda
Genetic Skin Disease Group and The Robin Eady National Diagnostic Epidermolysis Bullosa Research Lab
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DOPPING-HEPENSTAL Patricia
Genetic Skin Disease Group and The Robin Eady National Diagnostic Epidermolysis Bullosa Research Lab
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FASSIHI Hiva
Genetic Skin Disease Group and The Robin Eady National Diagnostic Epidermolysis Bullosa Research Lab
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Choy Yew
Genetics And Metabolism Unit Paediatric Institute Kuala Lumpur Hospital
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Ozoemena Linda
Genetic Skin Disease Group And The Robin Eady National Diagnostic Epidermolysis Bullosa Research Lab
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Fassihi Hiva
Genetic Skin Disease Group And The Robin Eady National Diagnostic Epidermolysis Bullosa Research Lab
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Wessagowit Vesarat
Genetic Skin Disease Group And The Robin Eady National Diagnostic Epidermolysis Bullosa Research Lab
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Dopping-hepenstal Patricia
Genetic Skin Disease Group And The Robin Eady National Diagnostic Epidermolysis Bullosa Research Lab
関連論文
- A novel OSMR mutation in familial primary localized cutaneous amyloidosis in a Japanese family
- Single nucleotide polymorphism in a commonly utilized LAMB3 primer sequence : Implications for mutation detection and haplotype analysis in junctional epidermolysis bullosa
- Neonatal diagnosis of Kindler syndrome
- Molecular Basis of Lipoid Proteinosis in Two Indian Siblings
- Focal dermal hypoplasia resulting from a new nonsense mutation, p. E300X, in the PORCN gene
- Human hair abnormalities resulting from inherited desmosome gene mutations
- Three-dimensional imaging reveals major changes in skin microvasculature in lipoid proteinosis and lichen sclerosus
- Normal and abnormal mechanisms of gene splicing and relevance to inherited skin diseases