S. L. Williamson

Lost in translation: translational interference from a recurrent mutation in exon 1 of MECP2 (2006)

Saxena, A., De Lagarde, D., Leonard, H., Williamson, S.L., Vasudevan, V., Christodoulou, J., ...

Copyright © 2006 by the BMJ Publishing Group Ltd.

Lost in translation: translational interference from a recurrent mutation in exon 1 of MECP2 (2006)

Saxena, A., De Lagarde, D., Leonard, H., Williamson, S.L., Vasudevan, V., Christodoulou, J., ...

Copyright © 2006 by the BMJ Publishing Group Ltd.

Mutations of CDKL5 cause a severe neurodevelopmental disorder with infantile spasms and mental retardation (2004)

Weaving, L. S., Christodoulou, J., Williamson, S. L., Friend, K. L., McKenzie, O. L.D., Archer, H., ...

Mutations of CDKL5 cause a severe neurodevelopmental disorder with infantile spasms and mental retardation (2004)

Weaving, L. S., Christodoulou, J., Williamson, S. L., Friend, K. L., McKenzie, O. L.D., Archer, H., ...

What Can The Learning And (2001)

F. M. Lamb, J. Bull, S. L. Williamson, F. Lamb

The Atkins Report acknowledges that academics best appreciate, assimilate and implement a pedagogic approach when it is presented to them within their own discipline.

New monoclonal antibodies to the T cell antigens CD4 and CD8. Production and characterization in formalin-fixed paraffin-embedded tissue.

Williamson, S. L., Steward, M., Milton, I., Parr, A., Piggott, N. H., Krajewski, A. S., ...

We have generated a recombinant protein representing part of the CD4 molecule and a peptide representing an epitope of predicted high antigenicity on the CD8 molecule and employed these to generate...