Single event transient propagation through digital optocouplers von Adell, P.C., Mion, O., Schrimpf, R.D., Chatry, C., Calvel, P., Melotte, M.R.

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SE372869 von MELOTTE R

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Chromosome instability is common in human cleavage-stage embryos von Vermeesch, Joris R, Vanneste, Evelyne, Voet, Thierry, Le Caignec, Cédric, Ampe, Michèle, Konings, Peter, Melotte, Cindy, Debrock, Sophie, Amyere, Mustapha, Vikkula, Miikka, Schuit, Frans, Fryns, Jean-Pierre, Verbeke, Geert, D'Hooghe, Thomas, Moreau, Yves

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A simplified checklist for the visual inspection of finished pharmaceutical products: a way to empower frontline health workers in the fight against poor-quality medicines von Schiavetti, B, Wynendaele, E, Melotte, V, Van der Elst, J, De Spiegeleer, B, Ravinetto, R

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TELEPHONE SUBSCRIBER APPARATUS von H. EBEL, H. LOSEHAND, G. WIGAND, R. MELOTTE

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TELEPHONE SUBSCRIBER APPARATUS von MELOTTE R, EBEL H, WIGAND G, LOSEHAND H

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DISPOSICAO DE CIRCUITO PARA UMA INSTALACAO TELEFONICA COM MEMORIA PARA OS NUMEROS DE CHAMADA DE TELEFONES QUE CHAMAM EM VAO von MELOTTE R, EBEL H, WIGAND G, LOSEHAND H

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The Quality of Medicines Used in Children and Supplied by Private Pharmaceutical Wholesalers in Kinshasa, Democratic Republic of Congo: A Prospective Survey von Schiavetti, Benedetta, Wynendaele, Evelien, De Spiegeleer, Bart, Mbinze, Geremie J, Kalenda, Nicodème, Marini, Roland, Melotte, Vera, Hasker, Epco, Meessen, Bruno, Ravinetto, Raffaella, Van der Elst, Josiane, Mutolo Ngeleka, Daniel

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Epstein-Barr virus and mismatch repair deficiency status differ between oesophageal and gastric cancer: A large multi-centre study von Hewitt, L.C., Inam, I.Z., Saito, Y., Yoshikawa, T., Quaas, A., Hoelscher, A., Bollschweiler, E., Fazzi, G.E., Melotte, V., Langley, R.E., Nankivell, M., Cunningham, D., Allum, W., Hutchins, G.G., Grabsch, H.I.

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ATP5PO levels regulate enteric nervous system development in zebrafish, linking Hirschsprung disease to Down Syndrome von Kuil, L.E., Chauhan, R.K., de Graaf, B.M., Cheng, W.W., Kakiailatu, N.J.M., Lasabuda, R., Verhaeghe, C., Windster, J.D., Schriemer, D., Azmani, Z., Brooks, A.S., Edie, S., Reeves, R.H., Eggen, B.J.L., Shepherd, I.T., Burns, A.J., Hofstra, R.M.W., Melotte, V., Brosens, E., Alves, M.M.

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What next for preimplantation genetic screening? High mitotic chromosome instability rate provides the biological basis for the low success rate von Vanneste, Evelyne, Voet, Thierry, Melotte, Cindy, Debrock, Sophie, Sermon, Karen, Staessen, Catherine, Liebaers, Inge, Fryns, Jean-Pierre, D'Hooghe, Thomas, Vermeesch, Joris R.

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Preimplantation genetic screening for aneuploidy of embryos after in vitro fertilization in women aged at least 35 years: a prospective randomized trial von Debrock, Sophie, Ph.D, Melotte, Cindy, M.Sc, Spiessens, Carl, Ph.D, Peeraer, Karen, M.D, Vanneste, Evelyne, M.Sc, Meeuwis, Luc, M.D, Meuleman, Christel, M.D, Frijns, Jean-Pierre, M.D., Ph.D, Vermeesch, Joris R., Ph.D, D'Hooghe, Thomas M., M.D., Ph.D

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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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Emerging patterns of cryptic chromosomal imbalance in patients with idiopathic mental retardation and multiple congenital anomalies: a new series of 140 patients and review of publ... von Menten, B, Maas, N, Thienpont, B, Buysse, K, Vandesompele, J, Melotte, C, de Ravel, T, Van Vooren, S, Balikova, I, Backx, L, Janssens, S, De Paepe, A, De Moor, B, Moreau, Y, Marynen, P, Fryns, J-P, Mortier, G, Devriendt, K, Speleman, F, Vermeesch, J R

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Genome-wide haplotyping embryos developing from 0PN and 1PN zygotes increases transferrable embryos in PGT-M von Destouni, Aspasia, Dimitriadou, Eftychia, Masset, Heleen, Debrock, Sophie, Melotte, Cindy, Van Den Bogaert, Kris, Zamani Esteki, Masoud, Ding, Jia, Voet, Thiery, Denayer, Ellen, de Ravel, Thomy, Legius, Eric, Meuleman, Christel, Peeraer, Karen, Vermeesch, Joris R

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Fusion of NUP214 to ABL1 on amplified episomes in T-cell acute lymphoblastic leukemia von Marynen, Peter, Hagemeijer, Anne, 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

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Rare Autosomal Trisomies and Adverse Perinatal Outcomes von Lannoo, Lore, Van Den Bogaert, Kris, Brison, Nathalie, Dehaspe, Luc, Dimitriadou, Eftychia, Fieuws, Steffen, Melotte, Cindy, Duquenne, Armelle, Parijs, Ilse, Sznajer, Yves, Vancoillie, Leen, Vandecruys, Hilde, Vermeesch, Joris R., Devriendt, Koen, Van Calsteren, Kristel

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Concurrent Whole-Genome Haplotyping and Copy-Number Profiling of Single Cells von Zamani Esteki, Masoud, Dimitriadou, Eftychia, Mateiu, Ligia, Melotte, Cindy, Van der Aa, Niels, Kumar, Parveen, Das, Rakhi, Theunis, Koen, Cheng, Jiqiu, Legius, Eric, Moreau, Yves, Debrock, Sophie, D’Hooghe, Thomas, Verdyck, Pieter, De Rycke, Martine, Sermon, Karen, Vermeesch, Joris R., Voet, Thierry

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Rare Autosomal Trisomies and Adverse Perinatal Outcomes von Lannoo, Lore, van den Bogaert, Kris, Brison, Nathalie, Dehaspe, Luc, Dimitriadou, Eftychia, Fieuws, Steffen, Melotte, Cindy, Duquenne, Armelle, Parijs, Ilse, Sznajer, Yves, Vancoillie, Leen, Vandecruys, Hilde, Vermeesch, Joris R, Devriendt, Koen, Van Calsteren, Kristel

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Human enteric glia diversity in health and disease: new avenues for the treatment of Hirschsprung disease von Windster, J D, Kakiailatu, N J M, Kuil, L E, Antanaviciute, A, Sacchetti, A, MacKenzie, K C, Peulen-Zink, J, Kan, T W, Bindels, E, de Pater, E, Doukas, M, van den Bosch, T P P, Yousefi, S, Barakat, T S, Meeussen, C, Sloots, C E J, Wijnen, R M H, Parikh, K, Boesmans, W, Melotte, V, Hofstra, R M W, Simmons, A, Alves, M M

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