For: |
Airaud F, Küry S, Valo I, Maury I, Bonneau D, Ingster O, Bezieau S. A |
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URL: | https://www.wjgnet.com/1007-9327/full/v18/i39/5635.htm |
Number | Citing Articles |
1 |
Tao Wang, Zsofia K. Stadler, Liying Zhang, Martin R. Weiser, Olca Basturk, Jaclyn F. Hechtman, Efsevia Vakiani, Lenard B. Saltz, David S. Klimstra, Jinru Shia. Immunohistochemical null-phenotype for mismatch repair proteins in colonic carcinoma associated with concurrent MLH1 hypermethylation and MSH2 somatic mutations. Familial Cancer 2018; 17(2): 225 doi: 10.1007/s10689-017-0031-9
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2 |
Elise Pierre-Noël, Fabrice Airaud, Estelle Cauchin, Céline Garrec, Ingrid Ricordeau, Clémence Michon, Olivier Kerdraon, Stéphane Bezieau, Caroline Abadie. A de novo pathogenic variant in the MSH6 gene in a 52 years-old woman. Familial Cancer 2022; 21(3): 319 doi: 10.1007/s10689-021-00274-w
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3 |
Clorinda Brignola, Sara Volorio, Giovanna De Vecchi, Daniela Zaffaroni, Valentina Dall’Olio, Frederique Mariette, Domenico Sardella, Fabio Capra, Stefano Signoroni, Emanuele Rausa, Marco Vitellaro, Valeria Pensotti, Maria Teresa Ricci. De novo germline pathogenic variant in Lynch Syndrome: A rare event or the tip of the iceberg?. Tumori Journal 2024; 110(1): 69 doi: 10.1177/03008916231197113
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4 |
Kristin Zajo, Susan I Colace, Danielle Mouhlas, Steven H Erdman. Lynch syndrome-associated colorectal cancer in a 16-year-old girl due to ade novo MSH2mutation. BMJ Case Reports 2020; 13(7): e233935 doi: 10.1136/bcr-2019-233935
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