ESHRE PGD Consortium ‘Best practice guidelines for clinical preimplantation genetic diagnosis (PGD) and preimplantation genetic screening (PGS)’ von Thornhill, A.R., deDie-Smulders, C.E., Geraedts, J.P., Harper, J.C., Harton, G.L., Lavery, S.A., Moutou, C., Robinson, M.D., Schmutzler, A.G., Scriven, P.N., Sermon, K.D., Wilton, L.

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Evaluation of exclusion prenatal and exclusion preimplantation genetic diagnosis for Huntington's disease in the Netherlands von van Rij, MC, de Die-Smulders, CEM, Bijlsma, EK, de Wert, GMWR, Geraedts, JP, Roos, RAC, Tibben, A

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Variable clinical manifestation of a novel missense mutation in the alpha-tropomyosin (TPM1) gene in familial hypertrophic cardiomyopathy von Jongbloed, Roselie J, Marcelis, Carlo L, Doevendans, Pieter A, Schmeitz-Mulkens, Judith M, Van Dockum, Willem G, Geraedts, Joep P, Smeets, Hubert J

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Association between Variants in the LEP Gene and Its Receptor (LEPR) with Birthweight and Pre-diabetic Phenotypes in Young Healthy Twins von NY Souren, ADC Paulussen, A Steyls, RJF Loos, AP Stassen, M Gielen, G Beunen, R Fagard, C Derom, R Vlietinck, JP Geraedts, MP Zeegers

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Chromosomal localization of transfected genes by a combination of hot banding and fluorescence in situ hybridization von De Vries, JE, Kornips, FH, Wiegant, J, Moerkerk, PM, Senden, N, Schutte, B, Geraedts, JP, Bosman, FT, Ten Kate, J

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Do guided internet-based interventions result in clinically relevant changes for patients with depression? An individual participant data meta-analysis von Karyotaki, Eirini, Ebert, David Daniel, Donkin, Liesje, Riper, Heleen, Twisk, Jos, Burger, Simone, Rozental, Alexander, Lange, Alfred, Williams, Alishia D., Zarski, Anna Carlotta, Geraedts, Anna, van Straten, Annemieke, Kleiboer, Annet, Meyer, Björn, Ünlü Ince, Burçin B., Buntrock, Claudia, Lehr, Dirk, Snoek, Frank J., Andrews, Gavin, Andersson, Gerhard, Choi, Isabella, Ruwaard, Jeroen, Klein, Jan Philipp, Newby, Jill M., Schröder, Johanna, Laferton, Johannes A.C., Van Bastelaar, Kim, Imamura, Kotaro, Vernmark, Kristofer, Boß, Leif, Sheeber, Lisa B., Kivi, Marie, Berking, Matthias, Titov, Nickolai, Carlbring, Per, Johansson, Robert, Kenter, Robin, Perini, Sarah, Moritz, Steffen, Nobis, Stephanie, Berger, Thomas, Kaldo, Viktor, Forsell, Yvonne, Lindefors, Nils, Kraepelien, Martin, Björkelund, Cecilia, Kawakami, Norito, Cuijpers, Pim

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Novel KCNQ1 and HERG missense mutations in Dutch long‐QT families von Jongbloed, R.J.E., Wilde, A.A.M., Geelen, J.L.M.C., Doevendans, P., Schaap, C., Van Langen, I., van Tintelen, J.P., Cobben, J.M., Beaufort‐Krol, G.C.M., Geraedts, J.P.M., Smeets, H.J.M.

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Disclosure of five breakpoints in a complex chromosome rearrangement by microdissection and FISH von Engelen, J J, Loots, W J, Albrechts, J C, Motoh, P C, Fryns, J P, Hamers, A J, Geraedts, J P

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Do guided internet-based interventions result in clinically relevant changes for patients with depression? An individual participant data meta-analysis von Karyotaki, E, Ebert, DD, Donkin, L, Riper, H, Twisk, J, Burger, S, Rozental, A, Lange, A, Williams, AD, Zarski, AC, Geraedts, A, van Straten, A, Kleiboer, A, Meyer, B, Ince, BÜ, Buntrock, C, Lehr, D, Snoek, FJ, Andrews, G, Andersson, G, Choi, I, Ruwaard, J, Klein, JP, Newby, JM, Schröder, J, Laferton, JAC, Van Bastelaar, K, Imamura, K, Vernmark, K, Boß, L, Sheeber, LB, Kivi, M, Berking, M, Titov, N, Carlbring, P, Johansson, R, Kenter, R, Perini, S, Moritz, S, Nobis, S, Berger, T, Kaldo, V, Forsell, Y, Lindefors, N, Kraepelien, M, Björkelund, C, Kawakami, N, Cuijpers, P

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The 11q; 22q translocation: a collaborative study of 20 new cases and analysis of 110 families von ISELIUS, L, LINDSTEN, J, DUTRILLAUX, B, FUKUSHIMA, Y, GERAETIS, J. P. M, DE GROUCHY, J, ZUFFARDI, O, AURIAS, A, FRACCARO, M, BASTARD, C, BOTTELLI, A. M, BUI, T.-H, CAUFIN, D, DALPRA, L, DELENDI, N

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Brief clinical report: a patient with dup(10p) del (8q) and Pendred syndrome von VAN WOUVE, J. P, WIJNANDS, M. C, MOURAD-BAARS, P. E. C, GERAEDTS, J. P. M, BEVERSTOCK, G. C, VAN DE KAMP, J. J. P

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