VP06.11: Difference in procedure‐related risk of miscarriage between early and mid‐trimester amniocentesis: a retrospective cohort study von Steinfort, K., Van Houtven, E., Loquet, P., Blaumeiser, B., Jacquemyn, Y.

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Additional causal SNRPE mutations in hereditary hypotrichosis simplex von Pan, C., Humbatova, A., Zheng, L., Cesarato, N., Grimm, C., Chen, F., Blaumeiser, B., Catalán‐Lambán, A., Patiño‐García, A., Fischer, U., Cheng, R., Li, Y., Yu, X., Yao, Z., Li, M., Betz, R.C.

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Investigation of selected cytokine genes suggests that IL2RA and the TNF/LTA locus are risk factors for severe alopecia areata von Redler, S., Albert, F., Brockschmidt, F.F., Herold, C., Hanneken, S., Eigelshoven, S., Giehl, K.A., Kruse, R., Lutz, G., Wolff, H., Blaumeiser, B., Böhm, M., Becker, T., Nöthen, M.M., Betz, R.C.

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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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Disclosure Pattern and Follow-Up After the Molecular Diagnosis of BRCA/CHEK2 Mutations von Kegelaers, D., Merckx, W., Odeurs, P., van den Ende, J., Blaumeiser, B.

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The R620W polymorphism in PTPN22 confers general susceptibility for the development of alopecia areata von Betz, R.C., König, K., Flaquer, A., Redler, S., Eigelshoven, S., Kortüm, A.-K., Hanneken, S., Hillmer, A., Tüting, T., Lambert, J., De Weert, J., Kruse, R., Lutz, G., Blaumeiser, B., Nöthen, M.M.

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New perspective on maintenance therapies for platinum- sensitive recurrent ovarian cancer in women with germline and somatic mutations in BRCA1 and BRCA2 genes von Vergote, I, Bours, V, Blaumeiser, B, Baurain, J-F

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Evaluation of RAD51C as cancer susceptibility gene in a large breast-ovarian cancer patient population referred for genetic testing von De Leeneer, K., Van Bockstal, M., De Brouwer, S., Swietek, N., Schietecatte, P., Sabbaghian, N., Van den Ende, J., Willocx, S., Storm, K., Blaumeiser, B., Van Asperen, C. J., Wijnen, J. T., Leunen, K., Legius, E., Michils, G., Matthijs, G., Blok, M. J., Gomez-Garcia, E., De Paepe, A., Tischkowitz, M., Poppe, B., Claes, K.

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Preconceptional care: a systematic review of the current situation and recommendations for the future von Braspenningx, S, Haagdorens, M, Blaumeiser, B, Jacquemyn, Y, Mortier, G

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The TRAF1/C5 locus confers risk for familial and severe alopecia areata von Redler, S., Brockschmidt, F.F., Forstbauer, L., Giehl, K.A., Herold, C., Eigelshoven, S., Hanneken, S., De Weert, J., Lutz, G., Wolff, H., Kruse, R., Blaumeiser, B., Böhm, M., Becker, T., Nöthen, M.M., Betz, R.C.

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P-718 Preimplantation genetic testing in Belgium: recommendations for the genetic centres von Fernandez Gallardo, E, De Rycke, M, Berckmoes, V, Verdyck, P, Dimitriadou, E, Tsuiko, O, Denayer, E, Baetens, M, Janssens, S, Symoens, S, Beckers, S, Blaumeiser, B, Pichon, B, Gonzalez-Merino, E, Billard, J M

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Adams-Oliver syndrome: clinical description of a four-generation family and exclusion of five candidate genes von Verdyck, P, Blaumeiser, B, Holder-Espinasse, M, Van Hul, W, Wuyts, W

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A new highly penetrant form of obesity due to deletions on chromosome 16p11.2 von Froguel, P, Beckmann, J. S, Walters, R. G, Jacquemont, S, Valsesia, A, de Smith, A. J, Martinet, D, Andersson, J, Falchi, M, Chen, F, Andrieux, J, Lobbens, S, Delobel, B, Stutzmann, F, El-Sayed Moustafa, J. S, Chèvre, J.-C, Lecoeur, C, Vatin, V, Bouquillon, S, Buxton, J. L, Boute, O, Holder-Espinasse, M, Cuisset, J.-M, Lemaitre, M.-P, Ambresin, A.-E, Brioschi, A, Gaillard, M, Giusti, V, Fellmann, F, Ferrarini, A, Hadjikhani, N, Campion, D, Guilmatre, A, Goldenberg, A, Calmels, N, Mandel, J.-L, Le Caignec, C, David, A, Isidor, B, Cordier, M.-P, Dupuis-Girod, S, Labalme, A, Sanlaville, D, Béri-Dexheimer, M, Jonveaux, P, Leheup, B, Õunap, K, Bochukova, E. G, Henning, E, Keogh, J, Ellis, R. J, MacDermot, K. D, van Haelst, M. M, Vincent-Delorme, C, Plessis, G, Touraine, R, Philippe, A, Malan, V, Mathieu-Dramard, M, Chiesa, J, Blaumeiser, B, Kooy, R. F, Caiazzo, R, Pigeyre, M, Balkau, B, Sladek, R, Bergmann, S, Mooser, V, Waterworth, D, Reymond, A, Vollenweider, P, Waeber, G, Kurg, A, Palta, P, Esko, T, Metspalu, A, Nelis, M, Elliott, P, Hartikainen, A.-L, McCarthy, M. I, Peltonen, L, Carlsson, L, Jacobson, P, Sjöström, L, Huang, N, Hurles, M. E, O'Rahilly, S, Farooqi, I. S, Männik, K, Jarvelin, M.-R, Pattou, F, Meyre, D, Walley, A. J, Coin, L. J. M, Blakemore, A. I. F

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Prenatally detected copy number variants in a national cohort: A postnatal follow‐up study von Muys, Joke, Jacquemyn, Yves, Blaumeiser, Bettina, Bourlard, Laura, Brison, Nathalie, Bulk, Saskia, Chiarappa, Patrizia, De Leener, Anne, De Rademaeker, Marjan, Désir, Julie, Destrée, Anne, Devriendt, Koenraad, Dheedene, Annelies, Duquenne, Armelle, Fieuw, Annelies, Fransen, Erik, Gatot, Jean‐Stéphane, Jamar, Mauricette, Janssens, Sandra, Kerstjens, Jorien, Keymolen, Kathelijn, Lederer, Damien, Menten, Björn, Pichon, Bruno, Rombout, Sonia, Sznajer, Yves, Van Den Bogaert, Ann, Van Den Bogaert, Kris, Vermeesch, Joris, Janssens, Katrien

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Parent-of-origin Effect in Alopecia Areata: A Large-scale Pedigree Study von Redler, Silke, Basmanav, F Buket Ü, Blaumeiser, Bettina, Bartels, Natalie Garcia, Lutz, Gerhard, Tafazzoli, Aylar, Kruse, Roland, Wolff, Hans, Böhm, Markus, Blume-Peytavi, Ulrike, Becker, Tim, Nöthen, Markus M, Betz, Regina C

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Preimplantation genetic testing in Belgium: recommendations for the genetic centres von Gallardo, E. Fernandez, de Rycke, M., Berckmoes, V., Verdyck, P., Dimitriadou, E., Tsuiko, O., Denayer, E., Baetens, M., Janssens, S., Symoens, S., Beckers, S., Blaumeiser, B., Pichon, B., Gonzalez-Merino, E., Billard, Jean-Marie

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Invasive papillary carcinoma of the male breast von Blaumeiser, B, Tjalma, W A A, Verslegers, I, De Schepper, A M, Buytaert, P

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New perspective on maintenance therapies for platinum- sensitive recurrent ovarian cancer in women with germline and somatic mutations in BRCA1 and BRCA2 genes von Vergote, Ignace, Bours, V, Blaumeiser, B, Baurain, J.-F

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Prenatal diagnosis of pentalogy of Cantrell: a case report von Jochems, L, Jacquemyn, Y, Blaumeiser, B

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Investigation of the functional variant c.-169T > C of the Fc receptor-like 3 (FCRL3) gene in alopecia areata von Schäfer, N., Blaumeiser, B., Becker, T., Freudenberg-Hua, Y., Hanneken, S., Eigelshoven, S., Schmael, C., Lambert, J., De Weert, J., Kruse, R., Nöthen, M. M., Betz, R. C.

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