ERCC2 mutations in two siblings with a severe trichothiodystrophy phenotype von Leemans, G., De Raeve, L., Keymolen, K.

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Chromosomal abnormalities after ICSI in relation to semen parameters: results in 1114 fetuses and 1391 neonates from a single center von Belva, F, Bonduelle, M, Buysse, A, Van den Bogaert, A, Hes, F, Roelants, M, Verheyen, G, Tournaye, H, Keymolen, K

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Preimplantation genetic testing with HLA matching: from counseling to birth and beyond von De Rycke, M, De Vos, A, Belva, F, Berckmoes, V, Bonduelle, M, Buysse, A, Keymolen, K, Liebaers, I, Nekkebroeck, J, Verdyck, P, Verpoest, W

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Parameters of poor prognosis in preimplantation genetic testing for monogenic disorders von Van Der Kelen, A, Santos-Ribeiro, S, De Vos, A, Verdyck, P, De Rycke, M, Berckmoes, V, Tournaye, H, Blockeel, C, De Vos, M, Hes, F J, Keymolen, K, Verpoest, W

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Factors influencing the clinical outcome of preimplantation genetic testing for polycystic kidney disease von Berckmoes, V, Verdyck, P, De Becker, P, De Vos, A, Verheyen, G, Van der Niepen, P, Verpoest, W, Liebaers, I, Bonduelle, M, Keymolen, K, De Rycke, M

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TUBA1A mutations: from isolated lissencephaly to familial polymicrogyria von Jansen, A C, Oostra, A, Desprechins, B, De Vlaeminck, Y, Verhelst, H, Régal, L, Verloo, P, Bockaert, N, Keymolen, K, Seneca, S, De Meirleir, L, Lissens, W

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Expanding the clinical spectrum of biallelic ZNF335 variants von Stouffs, K., Stergachis, A.B., Vanderhasselt, T., Dica, A., Janssens, S., Vandervore, L., Gheldof, A., Bodamer, O., Keymolen, K., Seneca, S., Liebaers, I., Jayaraman, D., Hill, H.E., Partlow, J.N., Walsh, C.A., Jansen, A.C.

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Xeroderma pigmentosum and leukaemia in two sisters von Pintens, S., Pierret, L., Keymolen, K., Gutermuth, J., De Raeve, L.

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The annual incidence of DiGeorge/velocardiofacial syndrome von Devriendt, K, Fryns, J P, Mortier, G, van Thienen, M N, Keymolen, K

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OC06.04: The Belgian approach to meet the challenge in interpreting prenatal microarray results von Muys, J., Blaumeiser, B., Janssens, K., Bandelier, C., Gatot, J., Van Den Bogaert, A., Vermeesch, J., Rombout, S., Menten, B., Pichon, B., Keymolen, K., Van Den Bogaert, K., Janssens, S., Caberg, J., Désir, J., Sznajer, Y., Destree, A., Jacquemyn, Y.

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PP05.6 – 2896: Genotype-phenotype correlations and counseling in carriers of Filamin A gene mutations von Keymolen, K, Stouffs, K, Gheldof, A, Seneca, S, Vanderhasselt, T, Jansen, A

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Loss of DNA-dependent dimerization of the transcription factor SOX9 as a cause for campomelic dysplasia von Sock, Elisabeth, Pagon, Roberta A., Keymolen, Kathelijn, Lissens, Willy, Wegner, Michael, Scherer, Gerd

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P137 – 2976: Two cases of Noonan syndrome: Genotype–phenotype correlation von De Rademaeker, M, Jansen, A, Gies, I, Matthijs, G, Caljon, B, Stouffs, K, Keymolen, K

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ERCC 2 mutations in two siblings with a severe trichothiodystrophy phenotype von Leemans, G., De Raeve, L., Keymolen, K.

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P-552 Analysis of the genomewide BAF profiles of selected SNPs allows reliable aneuploidy detection in preimplantation embryos, independent of haplotyping von Verdyck, P, Berckmoes, V, Keymolen, K, Olsen, C, De Rycke, M

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P-773 No impact of cleavage-stage or blastocyst-stage embryo biopsy on growth and health in children up to 2 years of age von Belva, F, Kondowe, F, De Vos, A, Keymolen, K, Buysse, A, Hes, F, Verpoest, W, De Rycke, M

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P-764 Is children’s health up to two years of age affected by embryo vitrification? von Belva, F, Blockeel, C, Roelants, M, Keymolen, K, Buysse, A, Verheyen, G, Tournaye, H, Hes, F, Van Landuyt, L

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Intervention during pregnancy and allergic disease in the offspring von Salvatore, S., Keymolen, K., Hauser, B., Vandenplas, Y.

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P-766 A systematic review and standardized clinical validation of re-vitrification and/or re-biopsy of human embryos for preimplantation genetic testing (PGT): the REPEAT study von Petrone, P, Li Piani, L, Brutto, M, De Vos, A, De Rycke, M  D R, Verdyck, P, Fernandez-Gallardo, E, Berckmoes, V, Keymolen, K, Roelens, C, De Munck, N, Hes, F, Conforti, A, Cimadomo, D, Verpoest, W

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Chromosomal abnormalities after ICSI in relation to semen parameters: results in 1114 fetuses and 1391 neonates from a single center von Belva, F, Bonduelle, M, Buysse, A, Van den Bogaert, A, Hes, F, Roelants, M, Verheyen, G, Tournaye, H, Keymolen, K

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