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Year | Number of Results |
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1989 | 1 |
2010 | 1 |
2013 | 1 |
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Breakpoint determination of 15 large deletions in Peutz-Jeghers subjects.
Hum Genet. 2010 Oct;128(4):373-82. doi: 10.1007/s00439-010-0859-7. Epub 2010 Jul 11.
Hum Genet. 2010.
PMID: 20623358
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.
Zheng B, et al.
Dig Dis Sci. 2013 Oct;58(10):2868-72. doi: 10.1007/s10620-013-2737-3. Epub 2013 Jul 27.
Dig Dis Sci. 2013.
PMID: 23892522
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Superoxide dismutase deficiency and the toxicity of the products of autooxidation of polyunsaturated fatty acids in yeast.
Biliński T, Litwińska J, Błaszczyński M, Bajus A.
Biliński T, et al.
Biochim Biophys Acta. 1989 Jan 23;1001(1):102-6. doi: 10.1016/0005-2760(89)90312-3.
Biochim Biophys Acta. 1989.
PMID: 2563227
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A novel mutation in the STK11 gene causes heritable Peutz-Jeghers syndrome - a case report.
Chen JH, Zheng JJ, Guo Q, Liu C, Luo B, Tang SB, Cheng JD, Huang EW.
Chen JH, et al.
BMC Med Genet. 2017 Feb 23;18(1):19. doi: 10.1186/s12881-017-0373-z.
BMC Med Genet. 2017.
PMID: 28231849
Free PMC article.
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