| |
| | Research Profile - Dr G Standen |
 | | Standen, G.R. and Bowen, D.J. (1993) Factor XIII A Bristol 1: detection of a nonsense mutation (Arg 171 → stop codon) in factor XIIIA subunit deficiency. |
 | | Wood, N., Standen, G.R., Bowen, D., Cumming, A., Lush, C., Lee, R. and Bidwell, J. (1996) UHG-based mutation screening in type 2B von Willebrands disease: detection of a candidate mutation Ser547Phe. |
 | | Aslam, S., Bowen, D., Mandalaki, T., Gialeraki, R. and Standen, G.R. (1996) Factor XIII deficiency due to a 13 base pair deletion in exon III of the A subunit gene. |
| www.bristol.ac.uk /cellmolmed/postgrad_research/standen_profile.html (389 words) |
|