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Bias in detection of instability of the (C)8 mononucleotide repeat of MSH6 in tumours from HNPCC patientsDE LEEUW, Wiljo J. F; VAN PUIJENBROEK, Marjo; MERX, Renee et al.Oncogene (Basingstoke). 2001, Vol 20, Num 43, pp 6241-6244, issn 0950-9232Article

Down-regulation of HLA-A expression correlates with a better prognosis in colorectal cancer patientsMENON, Anand G; MORREAU, Hans; TOLLENAAR, Rob A. E. M et al.Laboratory investigation. 2002, Vol 82, Num 12, pp 1725-1733, issn 0023-6837, 9 p.Article

Microsatellite instability, immunohistochemistry, and additional PMS2 staining in suspected hereditary nonpolyposis colorectal CancerDE JONG, Andrea E; VAN PUIJENBROEK, Marjo; VASEN, Hans F. A et al.Clinical cancer research. 2004, Vol 10, Num 3, pp 972-980, issn 1078-0432, 9 p.Article

Identification of Patients with (Atypical) MUTYH-Associated Polyposis by KRAS2 c.34G > T Prescreening Followed by MUTYH Hotspot Analysis in Formalin-Fixed Paraffin-Embedded TissueVAN PUIJENBROEK, Marjo; NIELSEN, Maartje; TOPS, Carli M. J et al.Clinical cancer research. 2008, Vol 14, Num 1, pp 139-142, issn 1078-0432, 4 p.Article

Genome-wide Allelic State Analysis on Flow-Sorted Tumor Fractions Provides an Accurate Measure of Chromosomal AberrationsCORVER, Willem E; MIDDELDORP, Anneke; VAN WEZEL, Tom et al.Cancer research (Chicago, Ill.). 2008, Vol 68, Num 24, pp 10333-10340, issn 0008-5472, 8 p.Article

Molecularanalysis of colorectal cancer tumors from patients with mismatch repair : Proficient hereditary nonpolyposis colorectal cancer suggests novel carcinogenic pathwaysSANCHEZ-DE-ABAJO, Ana; DE LA HOYA, Miguel; VAN PUIJENBROEK, Marjo et al.Clinical cancer research. 2007, Vol 13, Num 19, pp 5729-5735, issn 1078-0432, 7 p.Article

Molecular analysis of hereditary nonpolyposis colorectal cancer in the United States: High mutation detection rate among clinically selected families and characterization of an American founder genomic deletion of the MSH2 geneWAGNER, Anja; BARROWS, Alicia; MEIJERS-HEIJBOER, Hanne et al.American journal of human genetics. 2003, Vol 72, Num 5, pp 1088-1100, issn 0002-9297, 13 p.Article

Tumour-specific methylation of PTPRG intron 1 locus in sporadic and Lynch syndrome colorectal cancerVAN ROON, Eddy H. J; DE MIRANDA, Noël F. C. C; VAN NIEUWENHUIZEN, Merlijn P et al.European journal of human genetics. 2011, Vol 19, Num 3, pp 307-312, issn 1018-4813, 6 p.Article

Frequent mutations in the 3'-untranslated region of IFNCR1 lack functional impairment in microsatellite-unstable colorectal tumoursDIERSSEN, Jan Willem F; VAN PUIJENBROEK, Marjo; DEZENTJE, David A et al.European journal of human genetics. 2008, Vol 16, Num 10, pp 1235-1239, issn 1018-4813, 5 p.Article

Gene expression of parathyroid tumors: Molecular subclassification and identification of the potential malignant phenotypeHAVEN, Carola J; HOWELL, Viive M; ROBINSON, Bruce G et al.Cancer research (Baltimore). 2004, Vol 64, Num 20, pp 7405-7411, issn 0008-5472, 7 p.Article

Pancreatic carcinoma in carriers of a specific 19 base pair deletion of CDKN2A/p16 (p16-Leiden)DE VOS TOT NEDERVEEN CAPPEL, Wouter H; OFFERHAUS, G. Johan A; MORREAU, Hans et al.Clinical cancer research. 2003, Vol 9, Num 10, pp 3598-3605, issn 1078-0432, 8 p., 1Article