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Familial endometrial cancer in female carriers of MSH6 germline mutations.
Wijnen J, de Leeuw W, Vasen H, van der Klift H, Møller P, Stormorken A, Meijers-Heijboer H, Lindhout D, Menko F, Vossen S, Möslein G, Tops C, Bröcker-Vriends A, Wu Y, Hofstra R, Sijmons R, Cornelisse C, Morreau H, Fodde R. Wijnen J, et al. Nat Genet. 1999 Oct;23(2):142-4. doi: 10.1038/13773. Nat Genet. 1999. PMID: 10508506 No abstract available.
MSH2 genomic deletions are a frequent cause of HNPCC.
Wijnen J, van der Klift H, Vasen H, Khan PM, Menko F, Tops C, Meijers Heijboer H, Lindhout D, Møller P, Fodde R. Wijnen J, et al. Nat Genet. 1998 Dec;20(4):326-8. doi: 10.1038/3795. Nat Genet. 1998. PMID: 9843200 No abstract available.
BRCA1 genomic deletions are major founder mutations in Dutch breast cancer patients.
Petrij-Bosch A, Peelen T, van Vliet M, van Eijk R, Olmer R, Drüsedau M, Hogervorst FB, Hageman S, Arts PJ, Ligtenberg MJ, Meijers-Heijboer H, Klijn JG, Vasen HF, Cornelisse CJ, van 't Veer LJ, Bakker E, van Ommen GJ, Devilee P. Petrij-Bosch A, et al. Nat Genet. 1997 Nov;17(3):341-5. doi: 10.1038/ng1197-341. Nat Genet. 1997. PMID: 9354803 Free article.
Rapid detection of BRCA1 mutations by the protein truncation test.
Hogervorst FB, Cornelis RS, Bout M, van Vliet M, Oosterwijk JC, Olmer R, Bakker B, Klijn JG, Vasen HF, Meijers-Heijboer H, et al. Hogervorst FB, et al. Nat Genet. 1995 Jun;10(2):208-12. doi: 10.1038/ng0695-208. Nat Genet. 1995. PMID: 7663517
Extending the p16-Leiden tumour spectrum by respiratory tract tumours.
Oldenburg RA, de Vos tot Nederveen Cappel WH, van Puijenbroek M, van den Ouweland A, Bakker E, Griffioen G, Devilee P, Cornelisse CJ, Meijers-Heijboer H, Vasen HF, Morreau H. Oldenburg RA, et al. J Med Genet. 2004 Mar;41(3):e31. doi: 10.1136/jmg.2003.012336. J Med Genet. 2004. PMID: 14985402 Free PMC article. No abstract available.
226 results