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Stulp RP, Vos YJ, Mol B, Karrenbeld A, Raad M, Mijle HJVD, Sijmons RH. First report of a |
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| URL: | https://www.wjgnet.com/1007-9327/full/v12/i5/809.htm |
| Number | Citing Articles |
| 1 |
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| 2 |
Monika Morak, Andreas Laner, Michael Scholz, Trisari Madorf, Elke Holinski-Feder. Report on de-novo mutation in the MSH2 gene as a rare event in hereditary nonpolyposis colorectal cancer. European Journal of Gastroenterology & Hepatology 2008; 20(11) doi: 10.1097/MEG.0b013e328305e185
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| 3 |
Aung Ko Win, Mark A Jenkins, Daniel D Buchanan, Mark Clendenning, Joanne P Young, Graham G Giles, Jack Goldblatt, Barbara A Leggett, John L Hopper, Stephen N Thibodeau, Noralane M Lindor. Determining the frequency of de novo germline mutations in DNA mismatch repair genes. Journal of Medical Genetics 2011; 48(8) doi: 10.1136/jmedgenet-2011-100082
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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 a de novo MSH2 mutation. BMJ Case Reports 2020; 13(7) doi: 10.1136/bcr-2019-233935
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| 5 |
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) doi: 10.1007/s10689-021-00274-w
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| 6 |
Leeanne J. Mead, Mark A. Jenkins, Joanne Young, Simon G. Royce, Letitia Smith, D. James B. St. John, Finlay Macrae, Graham G. Giles, John L. Hopper, Melissa C. Southey. Microsatellite Instability Markers for Identifying Early-Onset Colorectal Cancers Caused by Germ-Line Mutations in DNA Mismatch Repair Genes. Clinical Cancer Research 2007; 13(10) doi: 10.1158/1078-0432.CCR-06-2174
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| 7 |
L Smith, A Tesoriero, L Mead, S Royce, G Grubb, J Young, G Giles, M Jenkins, F Macrae, JL Hopper, MC Southey. Large genomic alterations in hMSH2 and hMLH1 in early‐onset colorectal cancer: identification of a large complex de novo hMLH1 alteration. Clinical Genetics 2006; 70(3) doi: 10.1111/j.1399-0004.2006.00662.x
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| 8 |
Willemina R. Geurts‐Giele, Efraim H. Rosenberg, Anja van Rens, Monique E. van Leerdam, Winand N. Dinjens, Fonnet E. Bleeker. Somatic mosaicism by a de novo MLH1 mutation as a cause of Lynch syndrome. Molecular Genetics & Genomic Medicine 2019; 7(7) doi: 10.1002/mgg3.699
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