Nicholas C. M. Hearle
Section of Cancer Genetics
Institute of Cancer Research
Sutton
United Kingdom
Name/email consistency: high
- Sequence changes in predicted promoter elements of STK11/LKB1 are unlikely to contribute to Peutz-Jeghers syndrome. Hearle, N.C., Tomlinson, I., Lim, W., Murday, V., Swarbrick, E., Lim, G., Phillips, R., Lee, P., O'Donohue, J., Trembath, R.C., Morrison, P.J., Norman, A., Taylor, R., Hodgson, S., Lucassen, A., Houlston, R.S. BMC. Genomics (2005)
- Mapping of a translocation breakpoint in a Peutz-Jeghers hamartoma to the putative PJS locus at 19q13.4 and mutation analysis of candidate genes in polyp and STK11-negative PJS cases. Hearle, N., Lucassen, A., Wang, R., Lim, W., Ross, F., Wheeler, R., Moore, I., Shipley, J., Houlston, R. Genes. Chromosomes. Cancer (2004)