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Items: 1 to 20 of 125

1.

Novel and recurrent mutations of STK11 gene in six Chinese cases with Peutz-Jeghers syndrome.

Dai L, Fu L, Liu D, Zhang K, Wu Y, Meng H, Zhang B, Guan X, Guo H, Bai Y.

Dig Dis Sci. 2014 Aug;59(8):1856-61. doi: 10.1007/s10620-014-3077-7. Epub 2014 Mar 7.

PMID:
24604241
2.

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 25;15:166. doi: 10.1186/s12876-015-0397-9.

3.

Three novel mutations of STK11 gene in Chinese patients with Peutz-Jeghers syndrome.

Tan H, Mei L, Huang Y, Yang P, Li H, Peng Y, Chen C, Wei X, Pan Q, Liang D, Wu L.

BMC Med Genet. 2016 Nov 8;17(1):77.

4.

Analysis of STK11 gene variant in five Chinese patients with Peutz-Jeghers syndrome.

Zheng B, Pan J, Wang Y, Li M, Lian M, Zheng Y, Jin Y.

Dig Dis Sci. 2013 Oct;58(10):2868-72. doi: 10.1007/s10620-013-2737-3. Epub 2013 Jul 27.

PMID:
23892522
5.
6.

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. doi: 10.1007/s10620-009-0837-x. Epub 2009 Jun 9.

PMID:
19507030
7.

[Mutation analysis of STK11 gene in a Chinese family with Peutz-Jeghers syndrome].

Zhao X, Huang Y, Yang B, Zhao Y.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014 Jun;31(3):294-7. doi: 10.3760/cma.j.issn.1003-9406.2014.03.008. Chinese.

PMID:
24928005
8.

[Mutation analysis of STK11 gene coding region for 20 Chinese patients with Peutz-Jeghers syndrome].

Zhao X, Li Y, Ling Y, Chen H, Zhang B, Xia T, Zhou P.

Nan Fang Yi Ke Da Xue Xue Bao. 2012 Apr;32(4):511-4. Chinese.

PMID:
22543132
9.

A Clinical and Molecular Genetic Study in 11 Chinese Children With Peutz-Jeghers Syndrome.

Zheng B, Wang C, Jia Z, Liu Z, Li M, Jin Y, Pan J.

J Pediatr Gastroenterol Nutr. 2017 Apr;64(4):559-564. doi: 10.1097/MPG.0000000000001316.

PMID:
27467201
10.

Two novel STK11 mutations in three Chinese families with Peutz-Jeghers syndrome.

Zuo YG, Xu KJ, Su B, Ho MG, Liu YH.

Chin Med J (Engl). 2007 Jul 5;120(13):1183-6.

PMID:
17637250
11.

A novel mutation in STK11 gene is associated with Peutz-Jeghers syndrome in Chinese patients.

Wang Z, Chen Y, Wu B, Zheng H, He J, Jiang B.

BMC Med Genet. 2011 Dec 14;12:161. doi: 10.1186/1471-2350-12-161.

12.

Germline mutations of the STK11 gene in Korean Peutz-Jeghers syndrome patients.

Yoon KA, Ku JL, Choi HS, Heo SC, Jeong SY, Park YJ, Kim NK, Kim JC, Jung PM, Park JG.

Br J Cancer. 2000 Apr;82(8):1403-6.

13.

Exome sequencing revealed novel germline mutations in Chinese Peutz-Jeghers syndrome patients.

Wang HH, Xie NN, Li QY, Hu YQ, Ren JL, Guleng B.

Dig Dis Sci. 2014 Jan;59(1):64-71. doi: 10.1007/s10620-013-2875-7. Epub 2013 Oct 24.

PMID:
24154639
14.

A 23-Nucleotide Deletion in STK11 Gene Causes Peutz-Jeghers Syndrome and Malignancy in a Chinese Patient Without a Positive Family History.

Zhao ZY, Jiang YL, Li BR, Yang F, Li J, Jin XW, Ning SB, Sun SH.

Dig Dis Sci. 2017 Nov;62(11):3014-3020. doi: 10.1007/s10620-017-4741-5. Epub 2017 Oct 6.

PMID:
28986664
15.

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. doi: 10.1097/MD.0000000000008591.

16.

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 22;9:44. doi: 10.1186/1471-2350-9-44.

17.

A novel mutation in STK11 gene is associated with Peutz-Jeghers Syndrome in Indian patients.

Thakur N, Reddy DN, Rao GV, Mohankrishna P, Singh L, Chandak GR.

BMC Med Genet. 2006 Sep 30;7:73.

18.

Identification of a novel de novo STK11 mutation in a Chinese child with Peutz-Jeghers syndrome.

Liu WL, Li F, He ZX, Jiang HY, Ai R, Zhu XP, Chen XX, Ma HW.

J Int Med Res. 2011;39(5):2033-8.

PMID:
22118009
19.

First report of somatic mosaicism for mutations in STK11 in four patients with Peutz-Jeghers syndrome.

McKay V, Cairns D, Gokhale D, Mountford R, Greenhalgh L.

Fam Cancer. 2016 Jan;15(1):57-61. doi: 10.1007/s10689-015-9839-3.

PMID:
26386697
20.

[Mutations of the STK11 and FHIT genes among patients with Peutz-Jeghers syndrome].

Mao X, Zhang Y, Wang H, Mao G, Ning S.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016 Apr;33(2):186-90. doi: 10.3760/cma.j.issn.1003-9406.2016.02.013. Chinese.

PMID:
27060312

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