P. V. van Zon

Peptide-induced HLA-E expression in human PBMCs is dependent on peptide sequence and the HLA-E genotype.

M. Tilanus, H. Popeijus, J. Vanderlocht, 2015, Tissue antigens.

Targeted next-generation sequencing: a novel diagnostic tool for primary immunodeficiencies.

E. Cuppen, M. van der Burg, B. van der Zwaag, 2014, The Journal of allergy and clinical immunology.

De novo recurrent germline mutation of theBRCA2 gene in a patient with early onset breast cancer

M. Ausems, R. B. van der Luijt, C. Wárlám-Rodenhuis, 2001, Journal of medical genetics.

Discordant NIPT result in a viable trisomy‐21 pregnancy due to prolonged contribution to cfDNA by a demised trisomy‐14 cotwin

R. Hochstenbach, J. V. van Harssel, K. Lichtenbelt, 2018, Clinical Case Reports.

DNA analysis of AHI1, NPHP1 and CYCLIN D1 in Joubert syndrome patients from the Netherlands.

M. Nelen, R. Sinke, D. Lindhout, 2008, European journal of medical genetics.

Mutations in GRIP1 cause Fraser syndrome

P. Scambler, M. Vogel, E. Blair, 2012, Journal of Medical Genetics.

Cell-free fetal DNA in the maternal circulation originates from the cytotrophoblast: proof from an unique case

R. Hochstenbach, J. V. van Harssel, M. Oudijk, 2015, Clinical case reports.

Diagnostic value of a microsatellite DNA marker for copper toxicosis in West-European Bedlington terriers and incidence of the disease.

T. V. D. van den Ingh, J. Rothuizen, V. Yuzbasiyan-Gurkan, 1999, Animal genetics.

Unexplained False Negative Results in Noninvasive Prenatal Testing: Two Cases Involving Trisomies 13 and 18

R. Hochstenbach, J. V. van Harssel, T. Brouwer, 2015, Case reports in genetics.