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Triangular face and vascular malformation. The links to renal failure.
Wauters A, Dejagere T, Devriendt K, Vanrenterghem Y, Maes B. Wauters A, et al. Among authors: devriendt k. Nephrol Dial Transplant. 2003 Feb;18(2):436-9. doi: 10.1093/ndt/18.2.436. Nephrol Dial Transplant. 2003. PMID: 12543906 No abstract available.
A new approach to imprinting mutation detection in GNAS by Sequenom EpiTYPER system.
Izzi B, Decallonne B, Devriendt K, Bouillon R, Vanderschueren D, Levtchenko E, de Zegher F, Van den Bruel A, Lambrechts D, Van Geet C, Freson K. Izzi B, et al. Among authors: devriendt k. Clin Chim Acta. 2010 Dec 14;411(23-24):2033-9. doi: 10.1016/j.cca.2010.08.034. Epub 2010 Aug 31. Clin Chim Acta. 2010. PMID: 20807523
Enhanced MCP-1 Release in Early Autosomal Dominant Polycystic Kidney Disease.
Janssens P, Decuypere JP, De Rechter S, Breysem L, Van Giel D, Billen J, Hindryckx A, De Catte L, Baldewijns M, Claes KBM, Wissing KM, Devriendt K, Bammens B, Meyts I, Torres VE, Vennekens R, Mekahli D. Janssens P, et al. Among authors: devriendt k. Kidney Int Rep. 2021 Apr 6;6(6):1687-1698. doi: 10.1016/j.ekir.2021.03.893. eCollection 2021 Jun. Kidney Int Rep. 2021. PMID: 34169210 Free PMC article.
Partial duplications of the ATRX gene cause the ATR-X syndrome.
Thienpont B, de Ravel T, Van Esch H, Van Schoubroeck D, Moerman P, Vermeesch JR, Fryns JP, Froyen G, Lacoste C, Badens C, Devriendt K. Thienpont B, et al. Among authors: devriendt k. Eur J Hum Genet. 2007 Oct;15(10):1094-7. doi: 10.1038/sj.ejhg.5201878. Epub 2007 Jun 20. Eur J Hum Genet. 2007. PMID: 17579672
Haploinsufficiency of TAB2 causes congenital heart defects in humans.
Thienpont B, Zhang L, Postma AV, Breckpot J, Tranchevent LC, Van Loo P, Møllgård K, Tommerup N, Bache I, Tümer Z, van Engelen K, Menten B, Mortier G, Waggoner D, Gewillig M, Moreau Y, Devriendt K, Larsen LA. Thienpont B, et al. Among authors: devriendt k. Am J Hum Genet. 2010 Jun 11;86(6):839-49. doi: 10.1016/j.ajhg.2010.04.011. Epub 2010 May 20. Am J Hum Genet. 2010. PMID: 20493459 Free PMC article.
Presenting symptoms in adults with the 22q11 deletion syndrome.
Vogels A, Schevenels S, Cayenberghs R, Weyts E, Van Buggenhout G, Swillen A, Van Esch H, de Ravel T, Corveleyn P, Devriendt K. Vogels A, et al. Among authors: devriendt k. Eur J Med Genet. 2014 Mar;57(4):157-62. doi: 10.1016/j.ejmg.2014.02.008. Epub 2014 Feb 24. Eur J Med Genet. 2014. PMID: 24576609 Free article.
592 results