A de novo germline MLH1 mutation in a Lynch syndrome patient with discordant immunohistochemical and molecular biology test results

doi:10.3748/wjg.v18.i39.5635

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Oct 21, 2012 (publication date) through Nov 29, 2024

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World Journal of Gastroenterology

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1007-9327

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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA

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World J Gastroenterol. Oct 21, 2012; 18(39): 5635-5639
Published online Oct 21, 2012. doi: 10.3748/wjg.v18.i39.5635

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Figure 1 Pedigree. Family tree shows the segregation and clinical manifestations in the family with de novo Homo sapiens mutL homolog 1 mutation. N: Normal carrier status; M: Mutated carrier status.

Citation: Airaud F, Küry S, Valo I, Maury I, Bonneau D, Ingster O, Bezieau S. A de novo germline MLH1 mutation in a Lynch syndrome patient with discordant immunohistochemical and molecular biology test results. World J Gastroenterol 2012; 18(39): 5635-5639
URL: https://www.wjgnet.com/1007-9327/full/v18/i39/5635.htm
DOI: https://dx.doi.org/10.3748/wjg.v18.i39.5635