Vasen HF - Search Results

1

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

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

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

6

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

7

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

8

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

9

Familial adenomatous polyposis and its clinical surveillance.

Vasen HF, Griffioen G, Tops CM, van Haeringen A, Nagengast FM, van Leeuwen-Cornelisse IS, Khan PM, van Slooten EA. Vasen HF, et al. Neth J Med. 1993 Apr;42(3-4):105-8. Neth J Med. 1993. PMID: 8391128 Review. No abstract available.

10

APC mutation in the alternatively spliced region of exon 9 associated with late onset familial adenomatous polyposis.

van der Luijt RB, Vasen HF, Tops CM, Breukel C, Fodde R, Meera Khan P. van der Luijt RB, et al. Among authors: vasen hf. Hum Genet. 1995 Dec;96(6):705-10. doi: 10.1007/BF00210303. Hum Genet. 1995. PMID: 8522331

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