Vasen H - Search Results

1

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. Among authors: vasen h. Genomics. 1992 Aug;13(4):1162-8. doi: 10.1016/0888-7543(92)90032-n. Genomics. 1992. PMID: 1324223

2

Seven new mutations in hMSH2, an HNPCC gene, identified by denaturing gradient-gel electrophoresis.

Wijnen J, Vasen H, Khan PM, Menko FH, van der Klift H, van Leeuwen C, van den Broek M, van Leeuwen-Cornelisse I, Nagengast F, Meijers-Heijboer A, et al. Wijnen J, et al. Among authors: vasen h. Am J Hum Genet. 1995 May;56(5):1060-6. Am J Hum Genet. 1995. PMID: 7726159 Free PMC article.

3

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. Among authors: vasen h. Genomics. 1994 Mar 1;20(1):1-4. doi: 10.1006/geno.1994.1119. Genomics. 1994. PMID: 8020934

4

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. Among authors: vasen h. Am J Hum Genet. 1996 Feb;58(2):300-7. Am J Hum Genet. 1996. PMID: 8571956 Free PMC article.

5

Hereditary nonpolyposis colorectal cancer families not complying with the Amsterdam criteria show extremely low frequency of mismatch-repair-gene mutations.

Wijnen J, Khan PM, Vasen H, van der Klift H, Mulder A, van Leeuwen-Cornelisse I, Bakker B, Losekoot M, Møller P, Fodde R. Wijnen J, et al. Among authors: vasen h. Am J Hum Genet. 1997 Aug;61(2):329-35. doi: 10.1086/514847. Am J Hum Genet. 1997. PMID: 9311737 Free PMC article.

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

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

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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