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Scoliosis in association with the 22q11.2 deletion syndrome: an observational study.
Homans JF, Baldew VGM, Brink RC, Kruyt MC, Schlösser TPC, Houben ML, Deeney VFX, Crowley TB, Castelein RM, McDonald-McGinn DM. Homans JF, et al. Among authors: houben ml. Arch Dis Child. 2019 Jan;104(1):19-24. doi: 10.1136/archdischild-2018-314779. Epub 2018 Apr 7. Arch Dis Child. 2019. PMID: 29627765
Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome.
Davies RW, Fiksinski AM, Breetvelt EJ, Williams NM, Hooper SR, Monfeuga T, Bassett AS, Owen MJ, Gur RE, Morrow BE, McDonald-McGinn DM, Swillen A, Chow EWC, van den Bree M, Emanuel BS, Vermeesch JR, van Amelsvoort T, Arango C, Armando M, Campbell LE, Cubells JF, Eliez S, Garcia-Minaur S, Gothelf D, Kates WR, Murphy KC, Murphy CM, Murphy DG, Philip N, Repetto GM, Shashi V, Simon TJ, Suñer DH, Vicari S, Scherer SW; International 22q11.2 Brain and Behavior Consortium; Bearden CE, Vorstman JAS. Davies RW, et al. Nat Med. 2020 Dec;26(12):1912-1918. doi: 10.1038/s41591-020-1103-1. Epub 2020 Nov 9. Nat Med. 2020. PMID: 33169016 Free PMC article.
Ocular findings in 22q11.2 deletion syndrome: A systematic literature review and results of a Dutch multicenter study.
von Scheibler ENMM, van der Valk Bouman ES, Nuijts MA, Bauer NJC, Berendschot TTJM, Vermeltfoort P, Bok LA, van Eeghen AM, Houben ML, van Amelsvoort TAMJ, Boot E, van Egmond-Ebbeling MB. von Scheibler ENMM, et al. Among authors: houben ml. Am J Med Genet A. 2022 Feb;188(2):569-578. doi: 10.1002/ajmg.a.62556. Epub 2021 Nov 12. Am J Med Genet A. 2022. PMID: 34773366 Free PMC article.
22q11.2 Deletion Syndrome as a Human Model for Idiopathic Scoliosis.
de Reuver S, Homans JF, Schlösser TPC, Houben ML, Deeney VFX, Crowley TB, Stücker R, Pasha S, Kruyt MC, McDonald-McGinn DM, Castelein RM. de Reuver S, et al. Among authors: houben ml. J Clin Med. 2021 Oct 20;10(21):4823. doi: 10.3390/jcm10214823. J Clin Med. 2021. PMID: 34768342 Free PMC article.
38 results