Genome-wide equine preimplantation genetic testing enabled by simultaneous haplotyping and copy number detection von De Coster, T., Zhao, Y., Tšuiko, O., Demyda-Peyrás, S., Van Soom, A., Vermeesch, J. R., Smits, K.

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Clinical implementation of NIPT - technical and biological challenges von Brady, P., Brison, N., Van Den Bogaert, K., de Ravel, T., Peeters, H., Van Esch, H., Devriendt, K., Legius, E., Vermeesch, J.R.

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Fusion of NUP214 to ABL1 on amplified episomes in T-cell acute lymphoblastic leukemia von Graux, C., Cools, J., Melotte, C., Quentmeier, H., Ferrando, A., Levine, R., Vermeesch, J.R., Stul, M., Dutta, B., Boeckx, N., Bosly, A., Heimann, P., Uyttebroeck, A., Mentens, N., Somers, R., MacLeod, R.A.F., Drexler, H.G., Look, A.T., Gilliland, D.G., Michaux, L., Vandenberghe, P., Wlodarska, I., Marynen, Peter, Hagemeijer, Anne

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Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant von Hannes, F D, Sharp, A J, Mefford, H C, de Ravel, T, Ruivenkamp, C A, Breuning, M H, Fryns, J-P, Devriendt, K, Van Buggenhout, G, Vogels, A, Stewart, H, Hennekam, R C, Cooper, G M, Regan, R, Knight, S J L, Eichler, E E, Vermeesch, J R

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PGD for a complex chromosomal rearrangement by array comparative genomic hybridization von Vanneste, E., Melotte, C., Voet, T., Robberecht, C., Debrock, S., Pexsters, A., Staessen, C., Tomassetti, C., Legius, E., D'Hooghe, T., Vermeesch, J.R.

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Genotype–phenotype correlation in 21 patients with Wolf–Hirschhorn syndrome using high resolution array comparative genome hybridisation (CGH) von Maas, N M C, Van Buggenhout, G, Hannes, F, Thienpont, B, Sanlaville, D, Kok, K, Midro, A, Andrieux, J, Anderlid, B-M, Schoumans, J, Hordijk, R, Devriendt, K, Fryns, J-P, Vermeesch, J R

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Microarray analysis reveals abnormal chromosomal complements in over 70% of 14 normally developing human embryos von Mertzanidou, A., Wilton, L., Cheng, J., Spits, C., Vanneste, E., Moreau, Y., Vermeesch, J.R., Sermon, K.

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Mild Wolf-Hirschhorn syndrome: micro-array CGH analysis of atypical 4p16.3 deletions enables refinement of the genotype-phenotype map von Van Buggenhout, G, Melotte, C, Dutta, B, Froyen, G, Van Hummelen, P, Marynen, P, Matthijs, G, de Ravel, T, Devriendt, K, Fryns, J P, Vermeesch, J R

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17q21.31 microduplication patients are characterised by behavioural problems and poor social interaction von Grisart, B, Willatt, L, Destrée, A, Fryns, J-P, Rack, K, de Ravel, T, Rosenfeld, J, Vermeesch, J R, Verellen-Dumoulin, C, Sandford, R

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Holoprosencephaly and ZIC2 microdeletions: novel clinical and epidemiological specificities delineated von Chabchoub, E, Willekens, D, Vermeesch, JR, Fryns, J-P

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Genomewide copy number alteration screening of circulating plasma DNA: potential for the detection of incipient tumors von Lenaerts, L., Vandenberghe, P., Brison, N., Che, H., Neofytou, M., Verheecke, M., Leemans, L., Maggen, C., Dewaele, B., Dehaspe, L., Vanderschueren, S., Dierickx, D., Vandecaveye, V., Amant, F., Vermeesch, J.R.

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Modulation of Aneuploidy in Leishmania donovani during Adaptation to Different In Vitro and In Vivo Environments and Its Impact on Gene Expression von Dumetz, F, Imamura, H, Sanders, M, Seblova, V, Myskova, J, Pescher, P, Vanaerschot, M, Meehan, C J, Cuypers, B, De Muylder, G, Späth, G F, Bussotti, G, Vermeesch, J R, Berriman, M, Cotton, J A, Volf, P, Dujardin, J C, Domagalska, M A

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Recent developments in genetics and medically assisted reproduction: from research to clinical applications von Harper, J C, Aittomäki, K, Borry, P, Cornel, M C, de Wert, G, Dondorp, W, Geraedts, J, Gianaroli, L, Ketterson, K, Liebaers, I, Lundin, K, Mertes, H, Morris, M, Pennings, G, Sermon, K, Spits, C, Soini, S, van Montfoort, A P A, Veiga, A, Vermeesch, J R, Viville, S, Macek, Jr, M

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Preimplantation genetic diagnosis using fluorescent in situ hybridization for cancer predisposition syndromes caused by microdeletions von Vanneste, E., Melotte, C., Debrock, S., D’Hooghe, T., Brems, H., Fryns, J.P., Legius, E., Vermeesch, J.R.

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Distal limb deficiencies, micrognathia syndrome, and syndromic forms of split hand foot malformation (SHFM) are caused by chromosome 10q genomic rearrangements von Dimitrov, B I, de Ravel, T, Van Driessche, J, de Die-Smulders, C, Toutain, A, Vermeesch, J R, Fryns, J P, Devriendt, K, Debeer, P

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Single closed-tube quantitative real-time PCR assay with dual-labelled probes for improved sex determination of equine embryos von De Coster, T., Van Poucke, M., Bogado Pascottini, O., Angel-Velez, D., Van den Branden, E., Peere, S., Papas, M., Gerits, I., Govaere, J., Peelman, L., Vermeesch, J.R., Van Soom, A., Smits, K.

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Submicroscopic chromosomal imbalances detected by array-CGH are a frequent cause of congenital heart defects in selected patients von Thienpont, Bernard, Mertens, Luc, de Ravel, Thomy, Eyskens, Benedicte, Boshoff, Derize, Maas, Nicole, Fryns, Jean-Pierre, Gewillig, Marc, Vermeesch, Joris R., Devriendt, Koen

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The Human Cleavage Stage Embryo Is a Cradle of Chromosomal Rearrangements von Voet, T., Vanneste, E., Vermeesch, J.R.

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Exome sequencing identifies a recessive PIGN splice site mutation as a cause of syndromic Congenital Diaphragmatic Hernia von Brady, P.D, Moerman, Philippe, De Catte, Luc, Deprest, J, Devriendt, K, Vermeesch, J.R

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Mosaicism del(8p)/inv dup(8p) in a dysmorphic female infant: a mosaic formed by a meiotic error at the 8p OR gene and an independent terminal deletion event von Vermeesch, J R, Thoelen, R, Salden, I, Raes, M, Matthijs, G, Fryns, J-P

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