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APA Citation
Hearle, N. C. M., Rudd, M. F., Lim, W., Murday, V., Lim, A. G., Phillips, R. K., Lee, P. W., O'Donohue, J., Morrison, P. J., Norman, A., Hodgson, S. V., Lucassen, A., & Houlston, R. S. (2006). exonic STK11 deletions are not a rare cause of Peutz-Jeghers syndrome. Journal of medical genetics, 43(4), e15. http://access.bl.uk/ark:/81055/vdc_100135553915.0x00003d