Search Results - K. Devriendt
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Submicroscopic chromosomal imbalances detected by array-CGH are a frequent cause of congenital heart defects in selected patients by Bernard Thienpont, Luc Mertens, Thomy de Ravel, B. Eyskens, Derize Boshoff, N Maas, J. P. Fryns, Marc Gewillig, Joris Vermeesch, K. Devriendt
Published 2007Artigo -
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Exome sequencing identifies rare variants in multiple genes in atrioventricular septal defect by Lisa C.A. D’Alessandro, Saeed Al Turki, Ashok Kumar Manickaraj, Dorin Manase, Barbara J.M. Mulder, Lynn Bergin, Herschel Rosenberg, Tapas Mondal, Elaine Gordon, Jane Lougheed, John Smythe, K. Devriendt, Shoumo Bhattacharya, Hugh Watkins, Jamie Bentham, Sarah Bowdin, Matthew E. Hurles, Seema Mital
Published 2015Artigo -
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Spectrum of FOXL2 gene mutations in blepharophimosis-ptosis-epicanthus inversus (BPES) families demonstrates a genotype-phenotype correlation by Elfride De Baere, Michael J. Dixon, Kent W. Small, Ethylin Wang Jabs, Bart Leroy, K Devriendt, Y. Gillerot, Geert Mortier, Françoise Meire, Lionel Van Maldergem, Winnie Courtens, Helle Hjalgrim, Shangzhi Huang, I. Liebaers, Nicole Van Regemorter, Philippe Touraine, Verayuth Praphanphoj, Alain Verloès, Nitin Udar, Vivek S. Yellore, Meenal Chalukya, Svetlana Yelchits, Anne De Paepe, Frédérique Kuttenn, Marc Fellous, Reiner A. Veitia, Ludwine Messiaen
Published 2001Artigo
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