van Vliet M - Search Results

1

Allelotype of human breast carcinoma: a second major site for loss of heterozygosity is on chromosome 6q.

Devilee P, van Vliet M, van Sloun P, Kuipers Dijkshoorn N, Hermans J, Pearson PL, Cornelisse CJ. Devilee P, et al. Among authors: van sloun p, van vliet m. Oncogene. 1991 Sep;6(9):1705-11. Oncogene. 1991. PMID: 1681492

2

Fractional allelic imbalance in human breast cancer increases with tetraploidization and chromosome loss.

Cornelisse CJ, Kuipers-Dijkshoorn N, van Vliet M, Hermans J, Devilee P. Cornelisse CJ, et al. Among authors: van vliet m. Int J Cancer. 1992 Feb 20;50(4):544-8. doi: 10.1002/ijc.2910500408. Int J Cancer. 1992. PMID: 1537620

3

Frequent somatic imbalance of marker alleles for chromosome 1 in human primary breast carcinoma.

Devilee P, van Vliet M, Bardoel A, Kievits T, Kuipers-Dijkshoorn N, Pearson PL, Cornelisse CJ. Devilee P, et al. Among authors: van vliet m. Cancer Res. 1991 Feb 1;51(3):1020-5. Cancer Res. 1991. PMID: 1670997

4

Somatic genetic changes on chromosome 18 in breast carcinomas: is the DCC gene involved?

Devilee P, van Vliet M, Kuipers-Dijkshoorn N, Pearson PL, Cornelisse CJ. Devilee P, et al. Among authors: van vliet m. Oncogene. 1991 Feb;6(2):311-5. Oncogene. 1991. PMID: 2000224

5

Evidence for a gene on 17p13.3, distal to TP53, as a target for allele loss in breast tumors without p53 mutations.

Cornelis RS, van Vliet M, Vos CB, Cleton-Jansen AM, van de Vijver MJ, Peterse JL, Khan PM, Børresen AL, Cornelisse CJ, Devilee P. Cornelis RS, et al. Among authors: van de vijver mj, van vliet m. Cancer Res. 1994 Aug 1;54(15):4200-6. Cancer Res. 1994. PMID: 8033152

6

Allele loss patterns on chromosome 17q in 109 breast carcinomas indicate at least two distinct target regions.

Cornelis RS, Devilee P, van Vliet M, Kuipers-Dijkshoorn N, Kersenmaeker A, Bardoel A, Khan PM, Cornelisse CJ. Cornelis RS, et al. Among authors: van vliet m. Oncogene. 1993 Mar;8(3):781-5. Oncogene. 1993. PMID: 8437862

7

A gene subject to genomic imprinting and responsible for hereditary paragangliomas maps to chromosome 11q23-qter.

Heutink P, van der Mey AG, Sandkuijl LA, van Gils AP, Bardoel A, Breedveld GJ, van Vliet M, van Ommen GJ, Cornelisse CJ, Oostra BA, et al. Heutink P, et al. Among authors: van der mey ag, van gils ap, van ommen gj, van vliet m. Hum Mol Genet. 1992 Apr;1(1):7-10. doi: 10.1093/hmg/1.1.7. Hum Mol Genet. 1992. PMID: 1301144

8

HindIII polymorphism in the DCC gene.

Devilee P, van Vliet M, Cho KR, Vogelstein B. Devilee P, et al. Among authors: van vliet m. Nucleic Acids Res. 1991 Dec 25;19(24):6965. doi: 10.1093/nar/19.24.6965. Nucleic Acids Res. 1991. PMID: 1684845 Free PMC article.

9

Improved interpretation of complex chromosomal rearrangements by combined GTG banding and in situ suppression hybridization using chromosome-specific libraries and cosmid probes.

Smit VT, Wessels JW, Mollevanger P, Dauwerse JG, van Vliet M, Beverstock GC, Breuning MH, Devilee P, Raap AK, Cornelisse CJ. Smit VT, et al. Among authors: van vliet m. Genes Chromosomes Cancer. 1991 Jul;3(4):239-48. doi: 10.1002/gcc.2870030402. Genes Chromosomes Cancer. 1991. PMID: 1958589

10

Linkage to markers for the chromosome region 17q12-q21 in 13 Dutch breast cancer kindreds.

Devilee P, Cornelis RS, Bootsma A, Bardoel A, van Vliet M, van Leeuwen I, Cleton FJ, de Klein A, Lindhout D, Vasen HF, et al. Devilee P, et al. Among authors: van leeuwen i, van vliet m. Am J Hum Genet. 1993 Apr;52(4):730-5. Am J Hum Genet. 1993. PMID: 8096358 Free PMC article.

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