Tops CM - Search Results

1

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.

2

Molecular Profile of MSH6-Associated Colorectal Carcinomas Shows Distinct Features From Other Lynch Syndrome-Associated Colorectal Carcinomas.

Helderman NC, Van Der Werf-'t Lam AS; MSH6 TUMOR GROUP; Morreau H, Boot A, Van Wezel T, Nielsen M. Helderman NC, et al. Gastroenterology. 2023 Jul;165(1):271-274.e2. doi: 10.1053/j.gastro.2023.03.198. Epub 2023 Mar 15. Gastroenterology. 2023. PMID: 36931573 Free article. No abstract available.

3

APC mosaicism, not always isolated: two first-degree relatives with apparently distinct APC mosaicism.

Terlouw D, Hes FJ, Suerink M, Boot A, Langers AMJ, Tops CM, van Leerdam ME, van Asperen CJ, Rozen SG, Bijlsma EK, van Wezel T, Morreau H, Nielsen M. Terlouw D, et al. Among authors: tops cm. Gut. 2023 Nov;72(11):2186-2187. doi: 10.1136/gutjnl-2022-328540. Epub 2022 Oct 28. Gut. 2023. PMID: 36307181 No abstract available.

4

Discordant Staining Patterns and Microsatellite Results in Tumors of MSH6 Pathogenic Variant Carriers.

van der Werf-'t Lam AS, Terlouw D, Tops CM, van Kan MS, van Hest LP, Gille HJP, Duijkers FAM, Wagner A, Eikenboom EL, Letteboer TGW, de Jong MM, Bajwa-Ten Broeke SW, Bleeker FE, Gomez Garcia EB, de Wind N, van Wezel JT, Morreau H, Suerink M, Nielsen M. van der Werf-'t Lam AS, et al. Among authors: tops cm. Mod Pathol. 2023 Sep;36(9):100240. doi: 10.1016/j.modpat.2023.100240. Epub 2023 Jun 10. Mod Pathol. 2023. PMID: 37307877 Free article.

5

Molecular and Clinicopathologic Characterization of Mismatch Repair-Deficient Endometrial Carcinoma Not Related to MLH1 Promoter Hypermethylation.

Kaya M, Post CCB, Tops CM, Nielsen M, Crosbie EJ, Leary A, Mileshkin LR, Han K, Bessette P, de Boer SM, Jürgenliemk-Schulz IM, Lutgens L, Jobsen JJ, Haverkort MAD, Nout RA, Kroep J, Creutzberg CL, Smit VTHBM, Horeweg N, van Wezel T, Bosse T. Kaya M, et al. Among authors: tops cm. Mod Pathol. 2024 Mar;37(3):100423. doi: 10.1016/j.modpat.2024.100423. Epub 2024 Jan 6. Mod Pathol. 2024. PMID: 38191122 Free 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. 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. Hum Genet. 1991 Feb;86(4):365-8. doi: 10.1007/BF00201835. Hum Genet. 1991. PMID: 1671849

8

Four-base-pair deletion polymorphism at D5S71 (C11p11) linked to APC in the human chromosome 5q21-q22 region.

Breukel C, Tops CM, Khan PM. Breukel C, et al. Among authors: tops cm. Nucleic Acids Res. 1989 Dec 25;17(24):10512. doi: 10.1093/nar/17.24.10512. Nucleic Acids Res. 1989. PMID: 2557595 Free PMC article.

9

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

10

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

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