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Aug 16, 2018 (publication date) through Jun 2, 2024
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Publication Name
World Journal of Clinical Cases
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2307-8960
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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
| For: | Duan FX, Gu GL, Yang HR, Yu PF, Zhang Z. Must Peutz-Jeghers syndrome patients have the LKB1/STK11 gene mutation? A case report and review of the literature. World J Clin Cases 2018; 6(8): 224-232 [PMID: 30148152 DOI: 10.12998/wjcc.v6.i8.224] |
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| URL: | https://www.wjgnet.com/1007-9327/full/v6/i8/224.htm |
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| 2 |
Teng Li, Wensheng Lin, Yilei Zhao, Jianping Zhu, Tao Sun, Li Ren. Distinct promoter methylation patterns of LKB1 in the hamartomatous polyps of Peutz-Jeghers syndrome and its potential in gastrointestinal malignancy prediction. Orphanet Journal of Rare Diseases 2020; 15(1) doi: 10.1186/s13023-020-01502-9
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Evgeniya Kirakosyan, Maxim Lokhmatov. High-Tech Diagnostic Methods and Enteroscopic Treatment of Children with Peutz-Jeghers Syndrome. European Journal of Pediatric Surgery 2020; 30(06): 529 doi: 10.1055/s-0039-3400286
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Anuja Lipsa, Pradnya Kowtal, Rajiv Sarin. Novel germline STK11 variants and breast cancer phenotype identified in an Indian cohort of Peutz–Jeghers syndrome. Human Molecular Genetics 2019; 28(11): 1885 doi: 10.1093/hmg/ddz027
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Abel Decmann, Attila Patócs, Peter Igaz. Genetics of Endocrine Diseases and Syndromes. Experientia Supplementum 2019; 111: 105 doi: 10.1007/978-3-030-25905-1_7
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Li-Xin Jiang, Yu-Rui Chen, Zu-Xin Xu, Yu-Hui Zhang, Zhi Zhang, Peng-Fei Yu, Zhi-Wei Dong, Hai-Rui Yang, Guo-Li Gu. Peutz-Jeghers syndrome without <i>STK11</i> mutation may correlate with less severe clinical manifestations in Chinese patients. World Journal of Gastroenterology 2023; 29(21): 3302-3317 doi: 10.3748/wjg.v29.i21.3302
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