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Hyperkalemia in young children: blood pressure checked?
Hollander R, Mortier G, van Hoeck K. Hollander R, et al. Among authors: mortier g. Eur J Pediatr. 2016 Dec;175(12):2011-2013. doi: 10.1007/s00431-016-2782-y. Epub 2016 Sep 17. Eur J Pediatr. 2016. PMID: 27639857
Tetrasomy and pentasomy of the X chromosome.
Schoubben E, Decaestecker K, Quaegebeur K, Danneels L, Mortier G, Cornette L. Schoubben E, et al. Among authors: mortier g. Eur J Pediatr. 2011 Oct;170(10):1325-7. doi: 10.1007/s00431-011-1491-9. Epub 2011 May 18. Eur J Pediatr. 2011. PMID: 21590264
Evidence for autosomal dominant inheritance in prenatally diagnosed CHAOS.
Vanhaesebrouck P, De Coen K, Defoort P, Vermeersch H, Mortier G, Goossens L, Smets K, Zecic A, Vandaele S, De Baets F. Vanhaesebrouck P, et al. Among authors: mortier g. Eur J Pediatr. 2006 Oct;165(10):706-8. doi: 10.1007/s00431-006-0134-z. Epub 2006 Apr 27. Eur J Pediatr. 2006. PMID: 16642370
Fourteen new cases contribute to the characterization of the 7q11.23 microduplication syndrome.
Van der Aa N, Rooms L, Vandeweyer G, van den Ende J, Reyniers E, Fichera M, Romano C, Delle Chiaie B, Mortier G, Menten B, Destrée A, Maystadt I, Männik K, Kurg A, Reimand T, McMullan D, Oley C, Brueton L, Bongers EM, van Bon BW, Pfund R, Jacquemont S, Ferrarini A, Martinet D, Schrander-Stumpel C, Stegmann AP, Frints SG, de Vries BB, Ceulemans B, Kooy RF. Van der Aa N, et al. Among authors: mortier g. Eur J Med Genet. 2009 Mar-Jun;52(2-3):94-100. doi: 10.1016/j.ejmg.2009.02.006. Epub 2009 Feb 26. Eur J Med Genet. 2009. PMID: 19249392
A Panel-Based Sequencing Analysis of Patients with Paget's Disease of Bone Suggests Enrichment of Rare Genetic Variation in regulators of NF-κB Signaling and Supports the Importance of the 7q33 Locus.
De Ridder R, Vandeweyer G, Boudin E, Hendrickx G, Huybrechts Y, Cremers TC, Devogelaer JP, Mortier G, Fransen E, Van Hul W. De Ridder R, et al. Among authors: mortier g. Calcif Tissue Int. 2021 Dec;109(6):656-665. doi: 10.1007/s00223-021-00881-w. Epub 2021 Jun 25. Calcif Tissue Int. 2021. PMID: 34173013
Disfluency: it is not always stuttering.
Cosyns M, van Zaalen Y, Mortier G, Janssens S, Amez A, Van Damme J, Van Borsel J. Cosyns M, et al. Among authors: mortier g. Clin Genet. 2014 Mar;85(3):298-9. doi: 10.1111/cge.12144. Epub 2013 Apr 9. Clin Genet. 2014. PMID: 23565840 No abstract available.
374 results