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Infantile hypertrophic pyloric stenosis in patients with esophageal atresia.
Birth Defects Res. 2020 May 15;112(9):670-687. doi: 10.1002/bdr2.1683. Epub 2020 Apr 16.
Birth Defects Res. 2020.
PMID: 32298054
Boston type craniosynostosis: report of a second mutation in MSX2.
Florisson JM, Verkerk AJ, Huigh D, Hoogeboom AJ, Swagemakers S, Kremer A, Heijsman D, Lequin MH, Mathijssen IM, van der Spek PJ.
Florisson JM, et al. Among authors: huigh d.
Am J Med Genet A. 2013 Oct;161A(10):2626-33. doi: 10.1002/ajmg.a.36126. Epub 2013 Aug 15.
Am J Med Genet A. 2013.
PMID: 23949913
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CXorf56, a dendritic neuronal protein, identified as a new candidate gene for X-linked intellectual disability.
Verkerk AJMH, Zeidler S, Breedveld G, Overbeek L, Huigh D, Koster L, van der Linde H, de Esch C, Severijnen LA, de Vries BBA, Swagemakers SMA, Willemsen R, Hoogeboom AJM, van der Spek PJ, Oostra BA.
Verkerk AJMH, et al. Among authors: huigh d.
Eur J Hum Genet. 2018 Apr;26(4):552-560. doi: 10.1038/s41431-017-0051-9. Epub 2018 Jan 26.
Eur J Hum Genet. 2018.
PMID: 29374277
Free PMC article.
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Analytical Validation of SKY92 for the Identification of High-Risk Multiple Myeloma.
van Beers EH, Huigh D, Bosman L, de Best L, Kuiper R, Spaan M, van Duin M, Sonneveld P, Dumee B, van Vliet MH.
van Beers EH, et al. Among authors: huigh d.
J Mol Diagn. 2021 Jan;23(1):120-129. doi: 10.1016/j.jmoldx.2020.10.010. Epub 2020 Nov 2.
J Mol Diagn. 2021.
PMID: 33152501
Free article.
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Bridging a diagnostic Kawasaki disease classifier from a microarray platform to a qRT-PCR assay.
Kuiper R, Wright VJ, Habgood-Coote D, Shimizu C, Huigh D, Tremoulet AH, van Keulen D, Hoggart CJ, Rodriguez-Manzano J, Herberg JA, Kaforou M, Tempel D, Burns JC, Levin M.
Kuiper R, et al. Among authors: huigh d.
Pediatr Res. 2023 Feb;93(3):559-569. doi: 10.1038/s41390-022-02148-y. Epub 2022 Jun 22.
Pediatr Res. 2023.
PMID: 35732822
Free PMC article.
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