Mcgrath John | Genetic Skin Disease Group And The Robin Eady National Diagnostic Epidermolysis Bullosa Research Lab
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- Genetic Skin Disease Group And The Robin Eady National Diagnostic Epidermolysis Bullosa Research Labの論文著者
Genetic Skin Disease Group And The Robin Eady National Diagnostic Epidermolysis Bullosa Research Lab | 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