D. Huigh

Boston type craniosynostosis: Report of a second mutation in MSX2

M. Lequin, A. Kremer, A. Verkerk, 2013, American journal of medical genetics. Part A.

Bridging a diagnostic Kawasaki disease classifier from a microarray platform to a qRT-PCR assay

C. Hoggart, M. Kaforou, V. Wright, 2022, Pediatric Research.

Models for infantile hypertrophic pyloric stenosis development in patients with esophageal atresia

D. Tibboel, R. Hofstra, A. de Klein, 2019, bioRxiv.

Infantile hypertrophic pyloric stenosis in patients with esophageal atresia.

D. Tibboel, R. Hofstra, A. de Klein, 2020, Birth defects research.

Bridging a diagnostic Kawasaki disease classifier from a microarray platform to a qRT-PCR assay

C. Hoggart, M. Kaforou, V. Wright, 2022, Pediatric Research.

CXorf56, a dendritic neuronal protein, identified as a new candidate gene for X-linked intellectual disability

B. D. de Vries, L. Koster, B. Oostra, 2018, European Journal of Human Genetics.

Analytical validation of SKY92 for the identification of high-risk Multiple Myeloma.

P. Sonneveld, M. V. van Vliet, R. Kuiper, 2020, The Journal of molecular diagnostics : JMD.

CXorf56, a dendritic neuronal protein, identified as a new candidate gene for X-linked intellectual disability

B. D. de Vries, L. Koster, A. Verkerk, 2018, European Journal of Human Genetics.