Voûte PA - Search Results

1

Comparative genomic hybridization analysis of Wilms tumors.

Steenman M, Redeker B, de Meulemeester M, Wiesmeijer K, Voûte PA, Westerveld A, Slater R, Mannens M. Steenman M, et al. Among authors: voute pa. Cytogenet Cell Genet. 1997;77(3-4):296-303. doi: 10.1159/000134602. Cytogenet Cell Genet. 1997. PMID: 9284942

2

Allelic loss of chromosome 1p36 in neuroblastoma is of preferential maternal origin and correlates with N-myc amplification.

Caron H, van Sluis P, van Hoeve M, de Kraker J, Bras J, Slater R, Mannens M, Voûte PA, Westerveld A, Versteeg R. Caron H, et al. Among authors: voute pa. Nat Genet. 1993 Jun;4(2):187-90. doi: 10.1038/ng0693-187. Nat Genet. 1993. PMID: 8102298

3

Delineation and physical separation of novel translocation breakpoints on chromosome 1p in two genetically closely associated childhood tumors.

Steenman MJ, Zijlstra N, Kruitbosch DL, Wiesmeijer C, Larizza L, Voûte PA, Westerveld A, Mannens MM. Steenman MJ, et al. Among authors: voute pa. Cytogenet Cell Genet. 2000;88(3-4):289-95. doi: 10.1159/000015542. Cytogenet Cell Genet. 2000. PMID: 10828613

4

A cytogenetic study of Wilms' tumor.

Slater RM, de Kraker J, Voûte PA, Delemarre JF. Slater RM, et al. Among authors: voute pa. Cancer Genet Cytogenet. 1985 Jan 1;14(1-2):95-109. doi: 10.1016/0165-4608(85)90220-1. Cancer Genet Cytogenet. 1985. PMID: 2981155

5

1p36: every subband a suppressor?

Versteeg R, Caron H, Cheng NC, van der Drift P, Slater R, Westerveld A, Voûte PA, Delattre O, Laureys G, Van Roy N, et al. Versteeg R, et al. Among authors: voute pa. Eur J Cancer. 1995;31A(4):538-41. doi: 10.1016/0959-8049(95)00037-j. Eur J Cancer. 1995. PMID: 7576962 Review. No abstract available.

6

Evidence for two tumour suppressor loci on chromosomal bands 1p35-36 involved in neuroblastoma: one probably imprinted, another associated with N-myc amplification.

Caron H, Peter M, van Sluis P, Speleman F, de Kraker J, Laureys G, Michon J, Brugières L, Voûte PA, Westerveld A, et al. Caron H, et al. Among authors: voute pa. Hum Mol Genet. 1995 Apr;4(4):535-9. doi: 10.1093/hmg/4.4.535. Hum Mol Genet. 1995. PMID: 7633401

7

Recurrent 1;17 translocations in human neuroblastoma reveal nonhomologous mitotic recombination during the S/G2 phase as a novel mechanism for loss of heterozygosity.

Caron H, van Sluis P, van Roy N, de Kraker J, Speleman F, Voûte PA, Westerveld A, Slater R, Versteeg R. Caron H, et al. Among authors: voute pa. Am J Hum Genet. 1994 Aug;55(2):341-7. Am J Hum Genet. 1994. PMID: 8037211 Free PMC article.

8

Allelic loss of the short arm of chromosome 4 in neuroblastoma suggests a novel tumour suppressor gene locus.

Caron H, van Sluis P, Buschman R, Pereira do Tanque R, Maes P, Beks L, de Kraker J, Voûte PA, Vergnaud G, Westerveld A, Slater R, Versteeg R. Caron H, et al. Among authors: voute pa. Hum Genet. 1996 Jun;97(6):834-7. doi: 10.1007/BF02346199. Hum Genet. 1996. PMID: 8641706

9

Chromosome 1p allelic loss in neuroblastoma: prognosis, genomic imprinting and 1;17 translocations.

Caron H, van Sluis P, van Roy N, Beks L, Maes P, Pereira do Tanque R, Slater R, de Kraker J, Speleman F, Voûte PA, et al. Caron H, et al. Among authors: voute pa. Prog Clin Biol Res. 1994;385:35-42. Prog Clin Biol Res. 1994. PMID: 7972230 No abstract available.

10

Allelic loss of chromosome 1p as a predictor of unfavorable outcome in patients with neuroblastoma.

Caron H, van Sluis P, de Kraker J, Bökkerink J, Egeler M, Laureys G, Slater R, Westerveld A, Voûte PA, Versteeg R. Caron H, et al. Among authors: voute pa. N Engl J Med. 1996 Jan 25;334(4):225-30. doi: 10.1056/NEJM199601253340404. N Engl J Med. 1996. PMID: 8531999 Free article.

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