KZ2015026/Annual Project of Air Force General Hospital[Grants and Funding] - Search Results

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2019	1
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Sanger sequencing in exonic regions of STK11 gene uncovers a novel de-novo germline mutation (c.962_963delCC) associated with Peutz-Jeghers syndrome and elevated cancer risk: case report of a Chinese patient.

Zhao ZY, Jiang YL, Li BR, Yang F, Li J, Jin XW, Ning SB, Sun SH. Zhao ZY, et al. BMC Med Genet. 2017 Nov 15;18(1):130. doi: 10.1186/s12881-017-0471-y. BMC Med Genet. 2017. PMID: 29141581 Free PMC article.

Close and regular surveillance is key to prevent severe complications for Peutz-Jeghers syndrome patients without gastrointestinal polyps: case report of a novel STK11 mutation (c.471_472delCT) in a Chinese girl.

Zhao ZY, Jiang YL, Li BR, Li J, Jin XW, Yu ED, Ning SB. Zhao ZY, et al. BMC Surg. 2018 Apr 23;18(1):24. doi: 10.1186/s12893-018-0357-8. BMC Surg. 2018. PMID: 29685139 Free PMC article.

Early screening the small bowel is key to protect Peutz-Jeghers syndrome patients from surgery: a novel mutation c.243delG in STK11 gene.

Jiang YL, Zhao ZY, Li BR, Li J, Jin XW, Yu ED, Xu XD, Ning SB. Jiang YL, et al. BMC Gastroenterol. 2019 May 9;19(1):70. doi: 10.1186/s12876-019-0987-z. BMC Gastroenterol. 2019. PMID: 31072341 Free PMC article.

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