Tops CM - Search Results

1

The natural history of a combined defect in MSH6 and MUTYH in a HNPCC family.

van Puijenbroek M, Nielsen M, Reinards TH, Weiss MM, Wagner A, Hendriks YM, Vasen HF, Tops CM, Wijnen J, van Wezel T, Hes FJ, Morreau H. van Puijenbroek M, et al. Among authors: tops cm. Fam Cancer. 2007;6(1):43-51. doi: 10.1007/s10689-006-9103-y. Fam Cancer. 2007. PMID: 17039270

2

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. Am J Med Genet. 1992 Jul 15;43(5):888-93. doi: 10.1002/ajmg.1320430528. Am J Med Genet. 1992. PMID: 1322639

3

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. Hum Genet. 1991 Feb;86(4):365-8. doi: 10.1007/BF00201835. Hum Genet. 1991. PMID: 1671849

4

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. Lancet. 1989 Dec 9;2(8676):1361-3. doi: 10.1016/s0140-6736(89)91968-5. Lancet. 1989. PMID: 2574305

5

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: tops cm. Hum Genet. 1988 Jun;79(2):183-5. doi: 10.1007/BF00280563. Hum Genet. 1988. PMID: 2839409

6

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. Am J Med Genet. 1993 Sep 15;47(4):563-7. doi: 10.1002/ajmg.1320470425. Am J Med Genet. 1993. PMID: 8256823

7

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. Among authors: tops cm. Neth J Med. 1993 Apr;42(3-4):105-8. Neth J Med. 1993. PMID: 8391128 Review. No abstract available.

8

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: tops cm. Hum Genet. 1995 Dec;96(6):705-10. doi: 10.1007/BF00210303. Hum Genet. 1995. PMID: 8522331

9

Molecular genetic tests as a guide to surgical management of familial adenomatous polyposis.

Vasen HF, van der Luijt RB, Slors JF, Buskens E, de Ruiter P, Baeten CG, Schouten WR, Oostvogel HJ, Kuijpers JH, Tops CM, Meera Khan P. Vasen HF, et al. Among authors: tops cm. Lancet. 1996 Aug 17;348(9025):433-5. doi: 10.1016/s0140-6736(96)01340-2. Lancet. 1996. PMID: 8709782

10

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: tops cm. Hum Genet. 1996 Dec;98(6):727-34. doi: 10.1007/s004390050293. Hum Genet. 1996. PMID: 8931709

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