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Early onset Huntington disease: a neuronal degeneration syndrome.
Seneca S, Fagnart D, Keymolen K, Lissens W, Hasaerts D, Debulpaep S, Desprechins B, Liebaers I, De Meirleir L. Seneca S, et al. Among authors: keymolen k. Eur J Pediatr. 2004 Dec;163(12):717-21. doi: 10.1007/s00431-004-1537-3. Eur J Pediatr. 2004. PMID: 15338298
Post-zygotic origin of isochromosome 12p.
de Ravel TJ, Keymolen K, van Assche E, Wittevronghel I, Moerman P, Salden I, Matthijs G, Fryns JP, Vermeesch JR. de Ravel TJ, et al. Among authors: keymolen k. Prenat Diagn. 2004 Dec 15;24(12):984-8. doi: 10.1002/pd.956. Prenat Diagn. 2004. PMID: 15614858
Pregnancy outcome in carriers of Robertsonian translocations.
Keymolen K, Van Berkel K, Vorsselmans A, Staessen C, Liebaers I. Keymolen K, et al. Am J Med Genet A. 2011 Oct;155A(10):2381-5. doi: 10.1002/ajmg.a.33941. Epub 2011 Sep 9. Am J Med Genet A. 2011. PMID: 21910218
A prospective study of the clinical utility of prenatal chromosomal microarray analysis in fetuses with ultrasound abnormalities and an exploration of a framework for reporting unclassified variants and risk factors.
Brady PD, Delle Chiaie B, Christenhusz G, Dierickx K, Van Den Bogaert K, Menten B, Janssens S, Defoort P, Roets E, Sleurs E, Keymolen K, De Catte L, Deprest J, de Ravel T, Van Esch H, Fryns JP, Devriendt K, Vermeesch JR. Brady PD, et al. Among authors: keymolen k. Genet Med. 2014 Jun;16(6):469-76. doi: 10.1038/gim.2013.168. Epub 2013 Oct 31. Genet Med. 2014. PMID: 24177055 Free article.
94 results