Vasen HF - Search Results

1

Germline mutations in the 3' part of APC exon 15 do not result in truncated proteins and are associated with attenuated adenomatous polyposis coli.

van der Luijt RB, Meera Khan P, Vasen HF, Breukel C, Tops CM, Scott RJ, Fodde R. van der Luijt RB, et al. Among authors: vasen hf. Hum Genet. 1996 Dec;98(6):727-34. doi: 10.1007/s004390050293. Hum Genet. 1996. PMID: 8931709

2

Germline mutations in APC and MUTYH are responsible for the majority of families with attenuated familial adenomatous polyposis.

Nielsen M, Hes FJ, Nagengast FM, Weiss MM, Mathus-Vliegen EM, Morreau H, Breuning MH, Wijnen JT, Tops CM, Vasen HF. Nielsen M, et al. Among authors: vasen hf. Clin Genet. 2007 May;71(5):427-33. doi: 10.1111/j.1399-0004.2007.00766.x. Clin Genet. 2007. PMID: 17489848

3

Eight novel inactivating germ line mutations at the APC gene identified by denaturing gradient gel electrophoresis.

Fodde R, van der Luijt R, Wijnen J, Tops C, van der Klift H, van Leeuwen-Cornelisse I, Griffioen G, Vasen H, Khan PM. Fodde R, et al. Genomics. 1992 Aug;13(4):1162-8. doi: 10.1016/0888-7543(92)90032-n. Genomics. 1992. PMID: 1324223

4

Rapid detection of translation-terminating mutations at the adenomatous polyposis coli (APC) gene by direct protein truncation test.

van der Luijt R, Khan PM, Vasen H, van Leeuwen C, Tops C, Roest P, den Dunnen J, Fodde R. van der Luijt R, et al. Genomics. 1994 Mar 1;20(1):1-4. doi: 10.1006/geno.1994.1119. Genomics. 1994. PMID: 8020934

5

Majority of hMLH1 mutations responsible for hereditary nonpolyposis colorectal cancer cluster at the exonic region 15-16.

Wijnen J, Khan PM, Vasen H, Menko F, van der Klift H, van den Broek M, van Leeuwen-Cornelisse I, Nagengast F, Meijers-Heijboer EJ, Lindhout D, Griffioen G, Cats A, Kleibeuker J, Varesco L, Bertario L, Bisgaard ML, Mohr J, Kolodner R, Fodde R. Wijnen J, et al. Am J Hum Genet. 1996 Feb;58(2):300-7. Am J Hum Genet. 1996. PMID: 8571956 Free PMC article.

6

Genetic evidence that Turcot syndrome is not allelic to familial adenomatous polyposis.

Tops CM, Vasen HF, van Berge Henegouwen G, Simoons PP, van de Klift HM, van Leeuwen SJ, Breukel C, Fodde R, den Hartog Jager FC, Nagengast FM, et al. Tops CM, et al. Among authors: vasen hf. Am J Med Genet. 1992 Jul 15;43(5):888-93. doi: 10.1002/ajmg.1320430528. Am J Med Genet. 1992. PMID: 1322639

7

A new deletion polymorphism at D5S71 raises the linkage information on adenomatous polyposis coli: implications for presymptomatic diagnosis.

Tops CM, Breukel C, van der Klift HM, von Leeuwen IS, Wijnen JT, Griffioen G, Vasen HF, den Hartog Jager FC, Nagengast FM, Lamers CB, et al. Tops CM, et al. Among authors: vasen hf. Hum Genet. 1991 Feb;86(4):365-8. doi: 10.1007/BF00201835. Hum Genet. 1991. PMID: 1671849

8

Presymptomatic diagnosis of familial adenomatous polyposis by bridging DNA markers.

Tops CM, Wijnen JT, Griffioen G, von Leeuwen IS, Vasen HF, den Hartog Jager FC, Breukel C, Nagengast FM, van der Klift HM, Lamers CB, et al. Tops CM, et al. Among authors: vasen hf. Lancet. 1989 Dec 9;2(8676):1361-3. doi: 10.1016/s0140-6736(89)91968-5. Lancet. 1989. PMID: 2574305

9

Close linkage of a highly polymorphic marker (D5S37) to familial adenomatous polyposis (FAP) and confirmation of FAP localization on chromosome 5q21-q22.

Meera Khan P, Tops CM, vd Broek M, Breukel C, Wijnen JT, Oldenburg M, vd Bos J, van Leeuwen-Cornelisse IS, Vasen HF, Griffioen G, et al. Meera Khan P, et al. Among authors: vasen hf. Hum Genet. 1988 Jun;79(2):183-5. doi: 10.1007/BF00280563. Hum Genet. 1988. PMID: 2839409

10

Non-allelic heterogeneity of familial adenomatous polyposis.

Tops CM, van der Klift HM, van der Luijt RB, Griffioen G, Taal BG, Vasen HF, Khan PM. Tops CM, et al. Among authors: vasen hf. Am J Med Genet. 1993 Sep 15;47(4):563-7. doi: 10.1002/ajmg.1320470425. Am J Med Genet. 1993. PMID: 8256823

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