van de Vosse E - Search Results

1

Centromeric and noncentromeric ADE2-selectable fragmentation vectors for yeast artificial chromosomes in AB1380.

Heus JJ, de Winther MP, van de Vosse E, van Ommen GJ, den Dunnen JT. Heus JJ, et al. Among authors: de winther mp, van ommen gj, van de vosse e. Genome Res. 1997 Jun;7(6):657-60. doi: 10.1101/gr.7.6.657. Genome Res. 1997. PMID: 9199939 Free PMC article.

2

High-resolution mapping by YAC fragmentation of a 2.5-Mb Xp22 region containing the human RS, KFSD and CLS disease genes.

Van de Vosse E, Van der Bent P, Heus JJ, Van Ommen GJ, Den Dunnen JT. Van de Vosse E, et al. Among authors: van der bent p, van ommen gj. Mamm Genome. 1997 Jul;8(7):497-501. doi: 10.1007/s003359900483. Mamm Genome. 1997. PMID: 9195994

3

A CA-repeat polymorphism near DXS418 (P122).

Van De Vosse E, Booms PF, Vossen RH, Wapenaar MC, Van Ommen GJ, Den Dunnen JT. Van De Vosse E, et al. Among authors: van ommen gj. Hum Mol Genet. 1993 Dec;2(12):2202. doi: 10.1093/hmg/2.12.2202-a. Hum Mol Genet. 1993. PMID: 8111402 No abstract available.

4

Scanning for genes in large genomic regions: cosmid-based exon trapping of multiple exons in a single product.

Datson NA, van de Vosse E, Dauwerse HG, Bout M, van Ommen GJ, den Dunnen JT. Datson NA, et al. Among authors: van ommen gj, van de vosse e. Nucleic Acids Res. 1996 Mar 15;24(6):1105-11. doi: 10.1093/nar/24.6.1105. Nucleic Acids Res. 1996. PMID: 8604345 Free PMC article.

5

An Xp22.1-p22.2 YAC contig encompassing the disease loci for RS, KFSD, CLS, HYP and RP15: refined localization of RS.

Van de Vosse E, Bergen AA, Meershoek EJ, Oosterwijk JC, Gregory S, Bakker B, Weissenbach J, Coffey AJ, van Ommen GJ, Den Dunnen JT. Van de Vosse E, et al. Among authors: van ommen gj. Eur J Hum Genet. 1996;4(2):101-4. doi: 10.1159/000472177. Eur J Hum Genet. 1996. PMID: 8744027

6

Exclusion of PPEF as the gene causing X-linked juvenile retinoschisis.

van de Vosse E, Franco B, van der Bent P, Montini E, Orth U, Hanauer A, Tijmes N, van Ommen GJ, Ballabio A, den Dunnen JT, Bergen AA. van de Vosse E, et al. Among authors: van der bent p, van ommen gj. Hum Genet. 1997 Dec;101(2):235-7. doi: 10.1007/s004390050622. Hum Genet. 1997. PMID: 9402977

7

Variation of CNV distribution in five different ethnic populations.

White SJ, Vissers LE, Geurts van Kessel A, de Menezes RX, Kalay E, Lehesjoki AE, Giordano PC, van de Vosse E, Breuning MH, Brunner HG, den Dunnen JT, Veltman JA. White SJ, et al. Among authors: de menezes rx, van de vosse e. Cytogenet Genome Res. 2007;118(1):19-30. doi: 10.1159/000106437. Cytogenet Genome Res. 2007. PMID: 17901696

8

Significant linkage disequilibrium between the Huntington disease gene and the loci D4S10 and D4S95 in the Dutch population.

Skraastad MI, Van de Vosse E, Belfroid R, Höld K, Vegter-van der Vlis M, Sandkuijl LA, Bakker E, van Ommen GJ. Skraastad MI, et al. Among authors: van ommen gj, van de vosse e. Am J Hum Genet. 1992 Oct;51(4):730-5. Am J Hum Genet. 1992. PMID: 1415218 Free PMC article.

9

Molecular genetic analysis of two families with keratosis follicularis spinulosa decalvans: refinement of gene localization and evidence for genetic heterogeneity.

Oosterwijk JC, Richard G, van der Wielen MJ, van de Vosse E, Harth W, Sandkuijl LA, Bakker E, van Ommen GJ. Oosterwijk JC, et al. Among authors: van der wielen mj, van ommen gj, van de vosse e. Hum Genet. 1997 Oct;100(5-6):520-4. doi: 10.1007/s004390050546. Hum Genet. 1997. PMID: 9341865

10

Characterization of SCML1, a new gene in Xp22, with homology to developmental polycomb genes.

van de Vosse E, Walpole SM, Nicolaou A, van der Bent P, Cahn A, Vaudin M, Ross MT, Durham J, Pavitt R, Wilkinson J, Grafham D, Bergen AA, van Ommen GJ, Yates JR, den Dunnen JT, Trump D. van de Vosse E, et al. Among authors: van der bent p, van ommen gj. Genomics. 1998 Apr 1;49(1):96-102. doi: 10.1006/geno.1998.5224. Genomics. 1998. PMID: 9570953

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