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Cited by in CrossRef
For: Stulp RP, Vos YJ, Mol B, Karrenbeld A, Raad M, Mijle HJVD, Sijmons RH. First report of a de novo germline mutation in the MLH1 gene. World J Gastroenterol 2006; 12(5): 809-811 [PMID: 16521201 DOI: 10.3748/wjg.v12.i5.809]
URL: https://www.wjgnet.com/1007-9327/full/v12/i5/809.htm
Number Citing Articles
1
Chrystelle Colas, Florence Coulet, Magali Svrcek, Ada Collura, Jean-François Fléjou, Alex Duval, Richard Hamelin. Advances in Cancer Research 2012; 113: 121 doi: 10.1016/B978-0-12-394280-7.00004-X
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 cancerEuropean Journal of Gastroenterology & Hepatology 2008; 20(11): 1101 doi: 10.1097/MEG.0b013e328305e185
3
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 mutationBMJ Case Reports 2020; 13(7): e233935 doi: 10.1136/bcr-2019-233935
4
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 womanFamilial Cancer 2022; 21(3): 319 doi: 10.1007/s10689-021-00274-w
5
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 GenesClinical Cancer Research 2007; 13(10): 2865 doi: 10.1158/1078-0432.CCR-06-2174
6
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 alterationClinical Genetics 2006; 70(3): 250 doi: 10.1111/j.1399-0004.2006.00662.x
7
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 syndromeMolecular Genetics & Genomic Medicine 2019; 7(7) doi: 10.1002/mgg3.699