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Page 1
Prenatal vs postnatal diagnosis of 22q11.2 deletion syndrome: cardiac and noncardiac outcomes through 1 year of age.
Freud LR, Galloway S, Crowley TB, Moldenhauer J, Swillen A, Breckpot J, Borrell A, Vora NL, Cuneo B, Hoffman H, Gilbert L, Nowakowska B, Geremek M, Kutkowska-Kaźmierczak A, Vermeesch JR, Devriendt K, Busa T, Sigaudy S, Vigneswaran T, Simpson JM, Dungan J, Gotteiner N, Gloning KP, Digilio MC, Unolt M, Putotto C, Marino B, Repetto G, Fadic M, Garcia-Minaur S, Achón Buil A, Thomas MA, Fruitman D, Beecroft T, Hui PW, Oskarsdottir S, Bradshaw R, Criebaum A, Norton ME, Lee T, Geiger M, Dunnington L, Isaac J, Wilkins-Haug L, Hunter L, Izzi C, Toscano M, Ghi T, McGlynn J, Romana Grati F, Emanuel BS, Gaiser K, Gaynor JW, Goldmuntz E, McGinn DE, Schindewolf E, Tran O, Zackai EH, Yan Q, Bassett AS, Wapner R, McDonald-McGinn DM. Freud LR, et al. Among authors: swillen a. Am J Obstet Gynecol. 2024 Mar;230(3):368.e1-368.e12. doi: 10.1016/j.ajog.2023.09.005. Epub 2023 Sep 16. Am J Obstet Gynecol. 2024. PMID: 37717890
Middle and inner ear malformations in velocardiofacial syndrome.
Devriendt K, Swillen A, Schatteman I, Lemmerling M, Dhooge I. Devriendt K, et al. Among authors: swillen a. Am J Med Genet A. 2004 Dec 1;131(2):225-6. doi: 10.1002/ajmg.a.30326. Am J Med Genet A. 2004. PMID: 15389775 No abstract available.
Prevalence and Nature of Hearing Loss in 22q11.2 Deletion Syndrome.
Van Eynde C, Swillen A, Lambeens E, Verhaert N, Desloovere C, Luts H, Poorten VV, Devriendt K, Hens G. Van Eynde C, et al. Among authors: swillen a. J Speech Lang Hear Res. 2016 Jun 1;59(3):583-9. doi: 10.1044/2015_JSLHR-H-15-0098. J Speech Lang Hear Res. 2016. PMID: 27249537
Laterality preference and cognition: cross-syndrome comparison of patients with trisomy 21 (Down), del7q11.23 (Williams-Beuren) and del22q11.2 (DiGeorge or Velo-Cardio-Facial) syndromes.
Carlier M, Desplanches AG, Philip N, Stefanini S, Vicari S, Volterra V, Deruelle C, Fisch G, Doyen AL, Swillen A. Carlier M, et al. Among authors: swillen a. Behav Genet. 2011 May;41(3):413-22. doi: 10.1007/s10519-011-9465-2. Epub 2011 Apr 1. Behav Genet. 2011. PMID: 21455680
Social phenotypes in genetic syndromes.
Swillen A, de Ravel T, Oliver C. Swillen A, et al. J Intellect Disabil Res. 2012 Oct;56(10):919-21. doi: 10.1111/j.1365-2788.2012.01620.x. J Intellect Disabil Res. 2012. PMID: 22973833 No abstract available.
138 results