Does MSI-low exist? by Tomlinson, I, Halford, S, Aaltonen, L, Hawkins, N, Ward, R

MED12 exon 2 mutations are common in uterine leiomyomas from South African patients. by Mäkinen, N, Heinonen, H, Moore, S, Moore, S, Tomlinson, I, Tomlinson, I, van der Spuy, Z, van der Spuy, Z, Aaltonen, L, Aaltonen, L

The role of hypermethylation of the hMLH1 promoter region in HNPCC versus sporadic RER plus colorectal cancers by Wheeler, J, Loukola, A, Aaltonen, L, Mortensen, N, Bodmer, W

The role of hypermethylation of the hMLH1 promoter region in HNPCC versus MSI plus sporadic colorectal cancers by Wheeler, J, Loukola, A, Aaltonen, L, Mortensen, N, Bodmer, W

The role of hypermethylation of the hMLH1 promoter region in HNPCC versus MSI+ sporadic colorectal cancers. by Wheeler, J, Loukola, A, Aaltonen, L, Mortensen, N, Bodmer, W

MDM2 SNP309 accelerates colorectal tumour formation in women. by Bond, G, Menin, C, Bertorelle, R, Alhopuro, P, Aaltonen, L, Levine, A

Effect of SNP haplotypes associated with colorectal cancer risk on outcome by Walther, A, Sieber, O, Domingo, E, Jaeger, E, Johnstone, E, Orntoft, T, Aaltonen, L, Kerr, D, Tomlinson, I

Systematic search for enhancer elements and somatic allelic imbalance at seven low-penetrance colorectal cancer predisposition loci. by Niittymäki, I, Tuupanen, S, Li, Y, Järvinen, H, Mecklin, J, Tomlinson, I, Houlston, R, Karhu, A, Aaltonen, L

Comprehensive analysis of SMAD4 mutations and protein expression in juvenile polyposis: evidence for a distinct genetic pathway and polyp morphology in SMAD4 mutation carriers. by Woodford-Richens, K, Rowan, A, Poulsom, R, Bevan, S, Salovaara, R, Aaltonen, L, Houlston, R, Wright, N, Tomlinson, I

CDX2 mutations do not account for juvenile polyposis or Peutz-Jeghers syndrome and occur infrequently in sporadic colorectal cancers. by Woodford-Richens, K, Halford, S, Rowan, A, Bevan, S, Aaltonen, L, Wasan, H, Bicknell, D, Bodmer, W, Houlston, R, Tomlinson, I

7q deletion mapping and expression profiling in uterine fibroids. by Vanharanta, S, Wortham, N, Laiho, P, Sjöberg, J, Aittomäki, K, Arola, J, Tomlinson, I, Karhu, A, Arango, D, Aaltonen, L

CDX2 mutations do not account for juvenile polyposis or Peutz-Jeghers syndrome and occur infrequently in sporadic colorectal cancers by Woodford-Richens, K, Halford, S, Rowan, A, Bevan, S, Aaltonen, L, Hasan, H, Bicknell, D, Bodmer, W, Houlston, R, Tomlinson, I

Proportion and phenotype of MYH-associated colorectal neoplasia in a population-based series of Finnish colorectal cancer patients. by Enholm, S, Hienonen, T, Suomalainen, A, Lipton, L, Tomlinson, I, Kärjä, V, Eskelinen, M, Mecklin, J, Karhu, A, Järvinen, H, Aaltonen, L

Multiple colorectal adenomas, classic adenomatous polyposis, and germ-line mutations in MYH. by Sieber, O, Lipton, L, Crabtree, M, Heinimann, K, Fidalgo, P, Phillips, R, Bisgaard, M, Orntoft, T, Aaltonen, L, Hodgson, S, Thomas, H, Tomlinson, I

Definition of a minimal region of deletion of chromosome 7 in uterine leiomyomas by tiling-path microarray CGH and mutation analysis of known genes in this region. by Vanharanta, S, Wortham, N, Langford, C, El-Bahrawy, M, van der Spuy, Z, Sjöberg, J, Lehtonen, R, Karhu, A, Tomlinson, I, Aaltonen, L

Germline deletions of EXO1 do not cause colorectal tumors and lesions which are null for EXO1 do not have microsatellite instability. by Alam, N, Gorman, P, Jaeger, E, Kelsell, D, Leigh, I, Ratnavel, R, Murdoch, M, Houlston, R, Aaltonen, L, Roylance, R, Tomlinson, I

Mutations in the SMAD4/DPC4 gene in juvenile polyposis. by Howe, JR, Roth, S, Ringold, J, Summers, R, Järvinen, H, Sistonen, P, Tomlinson, I, Houlston, R, Bevan, S, Mitros, F, Stone, E, Aaltonen, L

Germline mutations of the LKB1 (STK11) gene in Peutz-Jeghers patients. by Wang, Z, Churchman, M, Avizienyte, E, McKeown, C, Davies, S, Evans, D, Ferguson, A, Ellis, I, Xu, W, Yan, Z, Aaltonen, L, Tomlinson, I

EPHB2 germline variants in patients with colorectal cancer or hyperplastic polyposis by Kokko, A, Laiho, P, Lehtonen, R, Korja, S, Carvajal-Carmona, L, Järvinen, H, Mecklin, J, Eng, C, Schleutker, J, Tomlinson, I, Vahteristo, P, Aaltonen, L

Localization of a susceptibility locus for Peutz-Jeghers syndrome to 19p using comparative genomic hybridization and targeted linkage analysis. by Hemminki, A, Tomlinson, I, Markie, D, Järvinen, H, Sistonen, P, Björkqvist, A, Knuutila, S, Salovaara, R, Bodmer, W, Shibata, D, de la Chapelle, A, Aaltonen, L