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Human Genetics|June 1, 1997
Physical mapping of the HOXA1 gene and the hnRPA2B1 gene in a YAC contig from human chromosome 7p14-p15L Van Laer, G Van Camp, E D Green, et al.
European Journal of Medical Genetics|September 8, 2020
Spondylo-epiphyseal dysplasia in two sibs due to a homozygous splicing variant in COL2A1N A Al-Sannaa, K P Hoornaert, L Van Laer, et al.
Clinical Genetics|May 17, 2018
Overlapping but distinct roles for NOTCH receptors in human cardiovascular diseaseJ A N Meester, A Verstraeten, M Alaerts, et al.
Clinical and Experimental Immunology|November 1, 1995
In vitro stimulation of peripheral blood mononuclear cells (PBMC) from HIV- and HIV+ chancroid patients by Haemophilus ducreyi antigensL Van Laer, J Vingerhoets, G Vanham, et al.
HNO|September 5, 2009
[Influence of exogenic factors on age-related hearing impairment]M Baur, E Fransen, A Tropitzsch, et al.
American Journal of Human Genetics|October 23, 1997
A novel locus for autosomal dominant nonsyndromic hearing loss, DFNA13, maps to chromosome 6pM R Brown, M S Tomek, L Van Laer, et al.
Clinical Genetics|October 14, 2014
Genetics of sudden cardiac death in the youngJ B Saenen, E M Van Craenenbroeck, D Proost, et al.
Genetic Testing|October 24, 2007
A new, easy, and rapid high-throughput detection method for the common GJB2 (CX26), 35delG mutationE Van Eyken, G Van Camp, J J Hendrickx, et al.
Gut|March 25, 2006
Molecular characterisation of non-absorptive and absorptive enterocytes in human small intestineN Gassler, D Newrzella, C Böhm, et al.
Scientific Reports|March 15, 2026
A new technique inducing mitral valve regurgitation as an experimental porcine model of volume-overload induced heart failureSven L Van Laer, Bo Goovaerts, Steven Laga, et al.
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