Benefit vs potential harm of genome‐wide prenatal cfDNA testing requires further investigation and should not be dismissed based on current data von Bekker, M. N., Henneman, L., Macville, M. V. E., Sistermans, E. A., Galjaard, R. J. H.

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Noninvasive detection of fetal trisomy 21: systematic review and report of quality and outcomes of diagnostic accuracy studies performed between 1997 and 2012 von Mersy, E, Smits, L J M, van Winden, L A A P, de Die-Smulders, C E M, Paulussen, A D C, Macville, M V E, Coumans, A B C, Frints, S G M

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Congenital hydrocephalus in clinical practice: A genetic diagnostic approach von Verhagen, J.M.A, Schrander-Stumpel, C.T.R.M, Krapels, I.P.C, de Die-Smulders, C.E.M, van Lint, F.H.M, Willekes, C, Weber, J.W, Gavilanes, A.W.D, Macville, M.V.E, Stegmann, A.P.A, Engelen, J.J.M, Bakker, J, Vos, Y.J, Frints, S.G.M

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Identification of Subgroups of High-grade Oligodendroglial Tumors by Comparative Genomic Hybridization von Jeuken, Judith W.M, Sprenger, Sandra H.E, Wesseling, Pieter, Macville, Merryn V.E, von Deimling, Andreas, Teepen, Hans L.J.M, van Overbeeke, Jacobus J, Boerman, Rudolf H

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P–381 Deciphering the genetic cause of recurrent and sporadic pregnancy loss von Essers, R, Acharya, G, Al-Nasiry, S, Brunner, H, Deligiannis, S P, Fonova, E A, Kurg, A, Lebedev, I N, Macville, M V E, Nikitina, T V, Salumets, A, Sazhenova, E A, Stevens, S J C, Tolmacheva, E N, Zaman. Esteki, M

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Prenatal cell-free DNA testing of women with pregnancy-associated cancer: a retrospective cross-sectional study von Heesterbeek, Catharina J., Tjan-Heijnen, Vivianne C.G., Heimovaara, Joosje H., Lenaerts, Liesbeth, Lok, Christianne, Vriens, Ingeborg J.H., Van Opstal, Diane, Boon, Elles M.J., Sie, Daoud, de Die-Smulders, Christine E.M., Amant, Frédéric, Macville, Merryn V.E., Sistermans, E.A., Henneman, L., Polstra, A., Voorhoeve, E., Zelderen-Bohla, S.L., Boon, E.M.J., Lombardi, M.P.R., Louwerens-Zintel, C., Smit, M., van Maarle, M.C., Tan-Sindhunata, M.B., van der Meij, K., Meij, H., Bax, C., Pajkrt, E., Linskens, I.H., Martin, L., Gitsels-van der Wal, J.T., Galjaard, R.J.H., Van Opstal, D., Srebniak, M.I., Jehee, F.M. Sarquis, Hollink, I.H.I.M., Sleutels, F., de Valk, W., Deelen, W.H., Joosten, A.M.S., Diderich, K.E.M., Redeker, M.E., Go, A.T.J.I., Knapen, M.F.C.M., Galjaard, S., Prinsen, A.K.E., Braat, A.P.G., Macville, M.V.E., Stevens, S.J.C., van der Wijngaard, A., Houben, L.H., van Esch-Lennarts, M.A.A., Hamers, L., Jetten, A.G.P., Ghesquiere, S.A.I., Koning, B. de, ZamaniEsteki, M., Heesterbeek, C.J., de Die-Smulders, C.E.M., Brunner, H., Pieters, M.J., Coumans, A.B.C., Smeets, D.F.C.M., Faas, B.H.W., Westra, D., Weiss, M.M., Derks-Prinsen, I., Feenstra, I., van Rij, M., Sikkel, E., Hoffer, M.J.V., Hollander, N.S. den, Verweij, E.J.T., Haak, M.C., Suijkerbuijk, R.F., Sikkema-Raddatz, B., van Langen, I.M., Bouman, K., Duin, L.K., Schuring-Blom, G.H., Lichtenbelt, K.D., Bekker, M.N., van der Ven, A.J.E.M., van Vliet-Lachotzki, E., Pot, J., van ‘t Padje, S., Bakker, I.M.C., Bradley, E.J.

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Saponin pre-treatment in pre-embedding electron microscopic in situ hybridization for detection of specific RNA sequences in cultured cells: a methodological study von Macville, MV, Wiesmeijer, KC, Dirks, RW, Fransen, JA, Raap, AK

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Reproductive (epi)genetics von Lynch, C., Tee, N., Rouse, H., Gordon, A., Sati, L., Zeiss, C., Soygur, B., Bassorgun, I., Goksu, E., Demir, R., McGrath, J., Groendahl, M. L., Thuesen, L., Andersen, A. N., Loft, A., Smitz, J., Adriaenssens, T., Vikesa, J., Borup, R., Mersy, E., Kisters, N., Macville, M. V. E., Engelen, J. J. M., Consortium, S.-E. N. N., Menheere, P. P. C. A., Geraedts, J. P., Coumans, A. B. C., Frints, S. G. M., Aledani, T., Assou, S., Traver, S., Ait-ahmed, O., Dechaud, H., Hamamah, S., Mizutani, E., Suzumori, N., Sugiyama, C., Hattori, Y., Sato, T., Ando, H., Ozaki, Y., Sugiura-Ogasawara, M., Wissing, M., Kristensen, S. G., Andersen, C. Y., Mikkelsen, A. L., Hoest, T., Velthut-Meikas, A., Simm, J., Metsis, M., Salumets, A., Palini, S., Galluzzi, L., De Stefani, S., Primiterra, M., Wells, D., Magnani, M., Bulletti, C., Vogt, P. H., Frank-Herrmann, P., Bender, U., Strowitzki, T., Besikoglu, B., Heidemann, P., Wunsch, L., Bettendorf, M., Jelinkova, L., Vilimova, S., Kosarova, M., Sebek, P., Volemanova, E., Kruzelova, M., Civisova, J., Svobodova, L., Sobotka, V., Mardesic, T., van de Werken, C., Santos, M. A., Eleveld, C., Laven, J. S. E., Baart, E. B., Pylyp, L. Y., Spinenko, L. A., Zukin, V. D., Perez-Sanz, J., Matorras, R., Arluzea, J., Bilbao, J., Gonzalez-Santiago, N., Yeh, N., Koff, A., Barlas, A., Romin, Y., Manova-Todorova, K., Hoz, C. D. l., Mauri, A. L., Nascimento, A. M., Vagnini, L. D., Petersen, C. G., Ricci, J.

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Individualized choice in prenatal diagnosis: the impact of karyotyping and standalone rapid aneuploidy detection on quality of life von Boormans, E. M. A., Birnie, E., Oepkes, D., Boekkooi, P. F., Bonsel, G. J., van Lith, J. M. M.

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Does confined placental mosaicism account for adverse perinatal outcomes in IVF pregnancies? von Jacod, B.C., Lichtenbelt, K.D., Schuring-Blom, G.H., Laven, J.S.E., van Opstal, D., Eijkemans, M.J.C., Macklon, N.S.

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The impact of rapid aneuploidy detection (RAD) in addition to karyotyping versus karyotyping on maternal quality of life von Boormans, E. M. A, Birnie, E., Oepkes, D., Bilardo, C. M., Wildschut, H. I. J., Creemers, J., Bonsel, G. J., Lith, J. M. M. van

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Session 49: Biomarkers of Early Pregnancy Outcome von Giles, J., Vidal, C., Bosch, E., Zuzuarregui, J. L., Aparicio, B., Ferrando, M., Oriol, B., Pellicer, A., Frints, S. G. M., Kisters, N., Nijhuis, J. G., Offermans, J. P., Macville, M. V. E., Engelen, J. J., de Wert, G. M., de Die-Smulders, C. E. M., Gereadts, J. P., Horne, A. W., Shaw, J. L. V., Duncan, W. C., Jabbour, H. N., Critchley, H. O. D., Lebedev, I., Sazhenova, E.

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AgarCyto: A Novel Cell-processing Method for Multiple Molecular Diagnostic Analyses of the Uterine Cervix von Kerstens, Harold M.J, Robben, Johanna C.M, Poddighe, Pino J, Melchers, Willem J.G, Boonstra, Henk, de Wilde, Petrus C.M, Macville, Merryn V.E, Hanselaar, Antonius G.J.M

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Monitoring morphology and signal during non-radioactive in situ hybridization procedures by reflection-contrast microscopy and transmission electron microscopy von Macville, MV, Van Dorp, AG, Wiesmeijer, KC, Dirks, RW, Fransen, JA, Raap, AK

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Absence of karyotype abnormalities in patients with familial urothelial cell carcinoma von Aben, Katja K.H, Macville, Merryn V.E, Smeets, Dominique F.C.M, Schoenberg, Mark P, Witjes, J.Alfred, Kiemeney, Lambertus A.L.M

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Spectral imaging of multi-color chromogenic dyes in pathological specimens von Macville, M V, Van der Laak, J A, Speel, E J, Katzir, N, Garini, Y, Soenksen, D, McNamara, G, de Wilde, P C, Hanselaar, A G, Hopman, A H, Ried, T

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Evaluation of pepsin treatment for electron microscopic RNA in situ hybridization on ultra-thin cryosections of cultured cells von Macville, M V, Van Dorp, A G, Dirks, R W, Fransen, J A, Raap, A K

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Absence of Heterozygosity Due to Template Switching during Replicative Rearrangements von Carvalho, Claudia M.B., Pfundt, Rolph, King, Daniel A., Lindsay, Sarah J., Zuccherato, Luciana W., Macville, Merryn V.E., Liu, Pengfei, Johnson, Diana, Stankiewicz, Pawel, Brown, Chester W., Shaw, Chad A., Hurles, Matthew E., Ira, Grzegorz, Hastings, P.J., Brunner, Han G., Lupski, James R.

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Experiences of pregnant women with genome-wide non-invasive prenatal testing in a national screening program von van der Meij, Karuna R M, van de Pol, Qiu Ying F, Bekker, Mireille N, Martin, Linda, Gitsels-van der Wal, Janneke, van Vliet-Lachotzki, Elsbeth H, Weiss, Janneke M, Galjaard, Robert-Jan H, Sistermans, Erik A, Macville, Merryn V E, Henneman, Lidewij

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Microarrays as a diagnostic tool in prenatal screening strategies: ethical reflection von de Jong, Antina, Dondorp, Wybo J., Macville, Merryn V. E., de Die-Smulders, Christine E. M., van Lith, Jan M. M., de Wert, Guido M. W. R.

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