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Deletions and loss-of-function variants in TP63 associated with orofacial clefting.
Khandelwal KD, van den Boogaard MH, Mehrem SL, Gebel J, Fagerberg C, van Beusekom E, van Binsbergen E, Topaloglu O, Steehouwer M, Gilissen C, Ishorst N, van Rooij IALM, Roeleveld N, Christensen K, Schoenaers J, Bergé S, Murray JC, Hens G, Devriendt K, Ludwig KU, Mangold E, Hoischen A, Zhou H, Dötsch V, Carels CEL, van Bokhoven H. Khandelwal KD, et al. Among authors: carels cel. Eur J Hum Genet. 2019 Jul;27(7):1101-1112. doi: 10.1038/s41431-019-0370-0. Epub 2019 Mar 8. Eur J Hum Genet. 2019. PMID: 30850703 Free PMC article. Clinical Trial.
A novel MSX1 mutation in hypodontia.
De Muynck S, Schollen E, Matthijs G, Verdonck A, Devriendt K, Carels C. De Muynck S, et al. Am J Med Genet A. 2004 Aug 1;128A(4):401-3. doi: 10.1002/ajmg.a.30181. Am J Med Genet A. 2004. PMID: 15264286
Syndrome of Hajdu-Cheney: three case reports of orofacial interest.
Vingerhoedt E, Bailleul-Forestier I, Fellus P, Schoenaers J, Frijns JP, Carels C. Vingerhoedt E, et al. Cleft Palate Craniofac J. 2010 Nov;47(6):645-53. doi: 10.1597/09-030. Epub 2010 Mar 1. Cleft Palate Craniofac J. 2010. PMID: 20500061
Vitamin A and clefting: putative biological mechanisms.
Ackermans MM, Zhou H, Carels CE, Wagener FA, Von den Hoff JW. Ackermans MM, et al. Nutr Rev. 2011 Oct;69(10):613-24. doi: 10.1111/j.1753-4887.2011.00425.x. Nutr Rev. 2011. PMID: 21967161 Review.
145 results