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4. Germline mutation analysis of STK11 gene using direct sequencing and multiplex ligation-dependent probe amplification assay in Korean children with Peutz-Jeghers syndrome. Yang HR; Ko JS; Seo JK Dig Dis Sci; 2010 Dec; 55(12):3458-65. PubMed ID: 20393878 [TBL] [Abstract][Full Text] [Related]
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11. STK11 domain XI mutations: candidate genetic drivers leading to the development of dysplastic polyps in Peutz-Jeghers syndrome. Wang Z; Wu B; Mosig RA; Chen Y; Ye F; Zhang Y; Gong W; Gong L; Huang F; Wang X; Nie B; Zheng H; Cui M; Wang Y; Wang J; Chen C; Polydorides AD; Zhang DY; Martignetti JA; Jiang B Hum Mutat; 2014 Jul; 35(7):851-8. PubMed ID: 24652667 [TBL] [Abstract][Full Text] [Related]
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