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Tumour-specific methylation of PTPRG intron 1 locus in sporadic and Lynch syndrome colorectal cancer.
van Roon EH, de Miranda NF, van Nieuwenhuizen MP, de Meijer EJ, van Puijenbroek M, Yan PS, Huang TH, van Wezel T, Morreau H, Boer JM. van Roon EH, et al. Among authors: van nieuwenhuizen mp, van puijenbroek m, van wezel t. Eur J Hum Genet. 2011 Mar;19(3):307-12. doi: 10.1038/ejhg.2010.187. Epub 2010 Dec 8. Eur J Hum Genet. 2011. PMID: 21150880 Free PMC article.
Mass spectrometry-based loss of heterozygosity analysis of single-nucleotide polymorphism loci in paraffin embedded tumors using the MassEXTEND assay: single-nucleotide polymorphism loss of heterozygosity analysis of the protein tyrosine phosphatase receptor type J in familial colorectal cancer.
van Puijenbroek M, Dierssen JW, Stanssens P, van Eijk R, Cleton-Jansen AM, van Wezel T, Morreau H. van Puijenbroek M, et al. Among authors: van eijk r, van wezel t. J Mol Diagn. 2005 Nov;7(5):623-30. doi: 10.1016/S1525-1578(10)60596-X. J Mol Diagn. 2005. PMID: 16258161 Free PMC article.
Reliable high-throughput genotyping and loss-of-heterozygosity detection in formalin-fixed, paraffin-embedded tumors using single nucleotide polymorphism arrays.
Lips EH, Dierssen JW, van Eijk R, Oosting J, Eilers PH, Tollenaar RA, de Graaf EJ, van't Slot R, Wijmenga C, Morreau H, van Wezel T. Lips EH, et al. Among authors: van t slot r, van eijk r, van wezel t. Cancer Res. 2005 Nov 15;65(22):10188-91. doi: 10.1158/0008-5472.CAN-05-2486. Cancer Res. 2005. PMID: 16288005
The natural history of a combined defect in MSH6 and MUTYH in a HNPCC family.
van Puijenbroek M, Nielsen M, Reinards TH, Weiss MM, Wagner A, Hendriks YM, Vasen HF, Tops CM, Wijnen J, van Wezel T, Hes FJ, Morreau H. van Puijenbroek M, et al. Among authors: van wezel t. Fam Cancer. 2007;6(1):43-51. doi: 10.1007/s10689-006-9103-y. Fam Cancer. 2007. PMID: 17039270
203 results