Browsing by Author "Lane, E. B."
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- ItemOpen AccessDNA based prenatal testing for the skin blistering disorder epidermolysis bullosa simplex(John Wiley & Sons, 2000) Rugg, E. L.; Baty, D.; Shemanko, Carrie S.; Magee, G.; Polak, S.; Bergman, R.; Kadar, T.; Boxer, M.; Falik-Zaccai, T.; Borochowitz, Z.; Lane, E. B.
- ItemOpen AccessEpidermolysis bullosa simplex in Scotland is caused by a spectrum of keratin mutations(Nature Publishing Group, 2007) Rugg, E. L.; Horn, H. M.; Smith, F. J.; Wilson, N. J.; Magee, G.; Shemanko, Carrie S.; Tidman, M. J.; Lane, E. B.
- ItemOpen AccessGeneration and characterization of cell lines expressing EBS keratin mutations: scratch assays show faster migration with more disruptive mutations(Blackwell Publishing, 2003) Morley, S. M.; D'Alessandro, M.; Sexton, C.; Rugg, E. L.; Navsaria, H.; Shemanko, Carrie S.; Hohl, D.; Heagerty, A. I.; Leigh, I. M.; Lane, E. B.
- ItemOpen AccessLaryngeal involvement in the Dowling-Meara variant of epidermolysis bullosa simplex with keratin mutations of severely disruptive potential(Blackwell Publishing, 2000) Shemanko, Carrie S.; Horn, H. M.; Keohane, S. G.; Hepburn, N.; Kerr, A. I.; Atherton, D. J.; Tidman, M. J.; Lane, E. B.
- ItemOpen AccessMutations in the plakophilin 1 gene result in ectodermal dysplasia/skin fragility syndrome(Nature Publishing Group, 1997) McGrath, J. A.; McMillan, J. R.; Shemanko, Carrie S.; Runswick, S. K.; Leigh, I. M.; Lane, E. B.; Garrod, D. R.; Eady, R. A.