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Exonic STK11 deletions are not a rare cause of Peutz-Jeghers syndrome.
J Med Genet. 2006 Apr;43(4):e15. doi: 10.1136/jmg.2005.036830.
J Med Genet. 2006.
PMID: 16582077
Free PMC article.
Sequence changes in predicted promoter elements of STK11/LKB1 are unlikely to contribute to Peutz-Jeghers syndrome.
Hearle NC, Tomlinson I, Lim W, Murday V, Swarbrick E, Lim G, Phillips R, Lee P, O'Donohue J, Trembath RC, Morrison PJ, Norman A, Taylor R, Hodgson S, Lucassen A, Houlston RS.
Hearle NC, et al.
BMC Genomics. 2005 Mar 17;6:38. doi: 10.1186/1471-2164-6-38.
BMC Genomics. 2005.
PMID: 15774015
Free PMC article.
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