Connexin mutations associated with palmoplantar keratoderma and profound deafness in a single family von Kelsell, DP, Wilgoss, AL, Richard, G, Stevens, HP, Munro, CS, Leigh, IM

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Diagnosis and confirmation of epidermolytic palmoplantar keratoderma by the identification of mutations in keratin 9 using denaturing high-performance liquid chromatography von Rugg, E.L., Common, J.E.A., Wilgoss, A., Stevens, H.P., Buchan, J., Leigh, I.M., Kelsell, D.P.

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Connexin mutations associated with palmoplantar keratoderma and profound deafness in a single family von Kelsell, D P, Wilgoss, A L, Richard, G, Stevens, H P, Munro, C S, Leigh, I M

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Connexin mutations associated with palmoplantar keratoderma and profound deafness in a single family von Kelsell, D P, Wilgoss, A L, Richard, G, Stevens, H P, Munro, C S, Leigh, I M

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Identification of a Novel Mutation R42P in the Gap Junction Protein β-3 Associated with Autosomal Dominant Erythrokeratoderma Variabilis von Wilgoss, Amanda, Leigh, Irene M., Kelsell, David P., Barnes, Michael R., Dopping-Hepenstal, Patricia, Eady, Robin A.J., Walter, Joanne M., Kennedy, Cameron T.C.

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Reality TV von Wilgoss, Peter

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Expression and Characterisation of Modified Human Cytochrome P450 IB l (CYPIBI) von Wilgoss, Amanda Louise

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Erratum: Connexin mutations associated with palmoplantar keratoderma and profound deafness in a single family von Kelsell, David P, Wilgoss, Amanda L, Richard, Gabriela, Stevens, Howard P, Munro, Colin S, Leigh, Irene M

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A systematic study of the electrical properties of Fe-doped InP single crystals von Cockayne, B., MacEwan, W. R., Brown, G. T., Wilgoss, W. H. E.

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A study of vapour phase epitaxy of indium phosphide von Fairhurst, K., Lee, D., Robertson, D. S., Parfitt, H. T., Wilgoss, W. H. E.

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The preparation of high purity epitaxial InP von Clarke, R.C., Joyce, B.D., Wilgoss, W.H.E.

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The Scattering Factor in n-Type InP von Hilsum, C., Rees, H. D., Wilgoss, W.

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