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4. Clinical characteristics and STK11 gene mutations in Chinese children with Peutz-Jeghers syndrome. Huang Z; Miao S; Wang L; Zhang P; Wu B; Wu J; Huang Y BMC Gastroenterol; 2015 Nov; 15():166. PubMed ID: 26607058 [TBL] [Abstract][Full Text] [Related]
5. A novel germline mutation (c.A527G) in STK11 gene causes Peutz-Jeghers syndrome in a Chinese girl: A case report. Zhao ZY; Jiang YL; Li BR; Yang F; Li J; Jin XW; Sun SH; Ning SB Medicine (Baltimore); 2017 Dec; 96(49):e8591. PubMed ID: 29245219 [TBL] [Abstract][Full Text] [Related]
6. A case of sporadic Peutz-Jeghers syndrome presenting as multiple intussusceptions. Gorji L; Huish G; Morgan J; Levy P J Surg Case Rep; 2022 Mar; 2022(3):rjac070. PubMed ID: 35280052 [TBL] [Abstract][Full Text] [Related]
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8. Peutz-Jeghers syndrome: an unusual cause of recurrent intussusception in a 7-year-old boy. Kılıç S; Atıcı A; Soyköse-Açıkalın Ö Turk J Pediatr; 2016; 58(5):535-537. PubMed ID: 28621096 [TBL] [Abstract][Full Text] [Related]
9. 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]
10. A novel de novo mutation in the serine-threonine kinase STK11 gene in a Korean patient with Peutz-Jeghers syndrome. Yoo JH; Yoo JH; Choi YJ; Kang JG; Sun YK; Ki CS; Lee KA; Choi JR BMC Med Genet; 2008 May; 9():44. PubMed ID: 18495044 [TBL] [Abstract][Full Text] [Related]
11. High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome. Aretz S; Stienen D; Uhlhaas S; Loff S; Back W; Pagenstecher C; McLeod DR; Graham GE; Mangold E; Santer R; Propping P; Friedl W Hum Mutat; 2005 Dec; 26(6):513-9. PubMed ID: 16287113 [TBL] [Abstract][Full Text] [Related]
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13. Multiple intestinal intussusceptions in Peutz-Jeghers' syndrome: a case report. Basak F; Kinaci E; Aksoy S; Sevinc M; Aren A Acta Chir Belg; 2010; 110(1):93-4. PubMed ID: 20306920 [TBL] [Abstract][Full Text] [Related]
14. Laparoscopic-assisted disinvagination and polypectomy for multiple intussusceptions induced by small intestinal polyps in patients with Peutz-Jeghers syndrome: a case report. Yamamoto M; Iwamoto K; Suzuki R; Mukai Y; Takeoka T; Asukai K; Shinno N; Hara H; Kanemura T; Nakai N; Hasegawa S; Sugimura K; Haraguchi N; Nishimura J; Wada H; Takahashi H; Matsuda C; Yasui M; Omori T; Miyata H; Ohue M; Murata M World J Surg Oncol; 2021 Jan; 19(1):22. PubMed ID: 33478478 [TBL] [Abstract][Full Text] [Related]
15. A De Novo mutation of STK11 gene in a Chinese patient with Peutz-Jeghers syndrome. Gao Y; Zhang FM; Huang S; Wang X; Zhang P; Huang XD; Ji GZ; Fan ZN Dig Dis Sci; 2010 Apr; 55(4):1032-6. PubMed ID: 19507030 [TBL] [Abstract][Full Text] [Related]
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17. STK11 status and intussusception risk in Peutz-Jeghers syndrome. Hearle N; Schumacher V; Menko FH; Olschwang S; Boardman LA; Gille JJ; Keller JJ; Westerman AM; Scott RJ; Lim W; Trimbath JD; Giardiello FM; Gruber SB; Offerhaus GJ; Rooij FW; Wilson JH; Hansmann A; Möslein G; Royer-Pokora B; Vogel T; Phillips RK; Spigelman AD; Houlston RS J Med Genet; 2006 Aug; 43(8):e41. PubMed ID: 16882735 [TBL] [Abstract][Full Text] [Related]
18. De novo germline mutation in the serine-threonine kinase STK11/LKB1 gene associated with Peutz-Jeghers syndrome. Hernan I; Roig I; Martin B; Gamundi MJ; Martinez-Gimeno M; Carballo M Clin Genet; 2004 Jul; 66(1):58-62. PubMed ID: 15200509 [TBL] [Abstract][Full Text] [Related]
19. Complete germline deletion of the STK11 gene in a family with Peutz-Jeghers syndrome. Le Meur N; Martin C; Saugier-Veber P; Joly G; Lemoine F; Moirot H; Rossi A; Bachy B; Cabot A; Joly P; Frébourg T Eur J Hum Genet; 2004 May; 12(5):415-8. PubMed ID: 14970844 [TBL] [Abstract][Full Text] [Related]
20. 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 Oct; 41(2):163-9. PubMed ID: 15287029 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]