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HARVARD Citation
Hearle, N. et al. (2006). Exonic STK11 deletions are not a rare cause of Peutz-Jeghers syndrome. Journal of medical genetics. 43 (4), p. e15. [Online].
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Hearle, N. et al. (2006). Exonic STK11 deletions are not a rare cause of Peutz-Jeghers syndrome. Journal of medical genetics. 43 (4), p. e15. [Online].