Walter van der Vliet
Overview
Explore the profile of Walter van der Vliet including associated specialties, affiliations and a list of published articles.
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Articles
6
Citations
193
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0
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Recent Articles
1.
Bus M, de Jong E, King J, van der Vliet W, Theelen J, Budowle B
Biotechniques
. 2021 Aug;
71(3):484-489.
PMID: 34350776
DNA analyses from challenging samples such as touch evidence, hairs and skeletal remains push the limits of the current forensic DNA typing technologies. Reverse complement PCR (RC-PCR) is a novel,...
2.
Kieser R, Bus M, King J, van der Vliet W, Theelen J, Budowle B
Forensic Sci Int Genet
. 2019 Dec;
44:102201.
PMID: 31786458
Reverse Complement PCR (RC-PCR) is an innovative, one-step PCR target enrichment technology adapted for the amplification of highly degraded (fragmented) DNA. It provides simultaneous amplification and tagging of a targeted...
3.
Hoischen A, Gilissen C, Arts P, Wieskamp N, van der Vliet W, Vermeer S, et al.
Hum Mutat
. 2010 Feb;
31(4):494-9.
PMID: 20151403
Massively parallel sequencing has tremendous diagnostic potential but requires enriched templates for sequencing. Here we report the validation of an array-based sequence capture method in genetically heterogeneous disorders. The model...
4.
Pfundt R, Smit F, Jansen C, Aalders T, Straatman H, van der Vliet W, et al.
Genes Chromosomes Cancer
. 2005 Apr;
43(3):273-83.
PMID: 15834941
The vast majority of androgen-dependent prostate tumors progress toward incurable, androgen-independent tumors. The identification of androgen-responsive genes, which are still actively transcribed in the tumors of patients who have undergone...
5.
Vissers L, de Vries B, Osoegawa K, Janssen I, Feuth T, Choy C, et al.
Am J Hum Genet
. 2003 Nov;
73(6):1261-70.
PMID: 14628292
Microdeletions and microduplications, not visible by routine chromosome analysis, are a major cause of human malformation and mental retardation. Novel high-resolution, whole-genome technologies can improve the diagnostic detection rate of...
6.
Veltman J, Jonkers Y, Nuijten I, Janssen I, van der Vliet W, Huys E, et al.
Am J Hum Genet
. 2003 May;
72(6):1578-84.
PMID: 12740760
Deletions of the long arm of chromosome 18 occur in approximately 1 in 10,000 live births. Congenital aural atresia (CAA), or narrow external auditory canals, occurs in approximately 66% of...