Reproductive Decision Support: Preferences and Needs of Couples at Risk for Hereditary Cancer and Clinical Geneticists von Reumkens, Kelly, van Oudheusden, A. J. G., Gietel-Habets, J. J. G., Tummers, M. H. E., de Die-Smulders, C. E. M., van Osch, L. A. D. M.

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BRCA1 mutation carriers have a lower number of mature oocytes after ovarian stimulation for IVF/PGD von Derks-Smeets, I. A. P., van Tilborg, T. C., van Montfoort, A., Smits, L., Torrance, H. L., Meijer-Hoogeveen, M., Broekmans, F., Dreesen, J. C. F. M., Paulussen, A. D. C., Tjan-Heijnen, V. C. G., Homminga, I., van den Berg, M. M. J., Ausems, M. G. E. M., de Rycke, M., de Die-Smulders, C. E. M., Verpoest, W., van Golde, R.

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Hereditary diseases and child wish: exploring motives, considerations, and the (joint) decision-making process of genetically at-risk couples von Severijns, Y., de Die-Smulders, C. E. M., Gültzow, T., de Vries, H., van Osch, L. A. D. M.

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Motives and considerations regarding PGT in couples carrying a structural chromosomal abnormality: a qualitative exploration von De Krom, G., Severijns, Y., Vlieg, W. L., Arens, Y. H. J. M., Van Golde, R. J. T., De Die-Smulders, C. E. M., Van Osch, L. A. D. M.

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Non-invasive prenatal diagnosis for aneuploidy: toward an integral ethical assessment von DE JONG, Antina, DONDORP, Wybo J, FRINTS, Suzanna G. M, DE DIE-SMULDERS, Christine E. M, DE WERT, Guido M. W. R

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Decision-making on preimplantation genetic diagnosis and prenatal diagnosis: a challenge for couples with hereditary breast and ovarian cancer von Derks-Smeets, I.A.P., Gietel-Habets, J.J.G., Tibben, A., Tjan-Heijnen, V.C.G., Meijer-Hoogeveen, M., Geraedts, J.P.M., van Golde, R., Gomez-Garcia, E., van den Bogaart, E., van Hooijdonk, M., de Die-Smulders, C.E.M., van Osch, L.A.D.M.

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Awareness and attitude regarding reproductive options of persons carrying a BRCA mutation and their partners von Gietel-Habets, J.J.G., de Die-Smulders, C.E.M., Derks-Smeets, I.A.P., Tibben, A., Tjan-Heijnen, V.C.G., van Golde, R., Gomez-Garcia, E., Kets, C.M., van Osch, L.A.D.M.

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Hereditary muscular dystrophies and the heart von Hermans, M.C.E, Pinto, Y.M, Merkies, I.S.J, de Die-Smulders, C.E.M, Crijns, H.J.G.M, Faber, C.G

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Age and causes of death in adult-onset myotonic dystrophy von DE DIE-SMULDERS, C. E. M, HÖWELER, C. J, THIJS, C, MIRANDOLLE, J. F, ANTEN, H. B, SMEETS, H. J. M, CHANDLER, K. E, GERAEDTS, J. P. M

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Preimplantation genetic testing for more than one genetic condition: clinical and ethical considerations and dilemmas von van der Schoot, V, Dondorp, W, Dreesen, J C F M, Coonen, E, Paulussen, A D C, de Wert, G, de Die-Smulders, C E M

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PGD to reduce reproductive risk: the case of mitochondrial DNA disorders von Bredenoord, A.L., Dondorp, W., Pennings, G., De Die-Smulders, C.E.M., De Wert, G.

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The cognitive and socio-emotional development of 5-year-old children born after PGD von Heijligers, M, Verheijden, L M M, Jonkman, L M, van der Sangen, M, Meijer-Hoogeveen, M, Arens, Y, van der Hoeven, M A, de Die-Smulders, C E M

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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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To what extent do decision aids for prenatal screening and diagnosis address involvement of partners in decision-making? - An environmental scan von Severijns, Y., van der Linden, H., de Die-Smulders, C.E.M., Hoving, C., Jansen, J., van Osch, L.A.D.M.

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Support needs of couples with hereditary breast and ovarian cancer during reproductive decision making von Gietel‐Habets, J.J.G., Die‐Smulders, C.E.M., Derks‐Smeets, I.A.P., Tibben, A., Tjan‐Heijnen, V.C.G., Golde, R., Gomez‐Garcia, E., Osch, L.A.D.M.

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Recurrent miscarriage in translocation carriers: no differences in clinical characteristics between couples who accept and couples who decline PGD von De Krom, G., Arens, Y.H.J.M., Coonen, E., Van Ravenswaaij-Arts, C.M.A., Meijer-Hoogeveen, M., Evers, J.L.H., Van Golde, R.J.T., De Die-Smulders, C.E.M.

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Reproductive options for prospective parents in families with Huntington's disease: clinical, psychological and ethical reflections von de Die-Smulders, C E M, de Wert, G M W R, Liebaers, I, Tibben, A, Evers-Kiebooms, G

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Professionals' knowledge, attitude and referral behaviour of preimplantation genetic diagnosis for hereditary breast and ovarian cancer von Gietel-Habets, J.J.G., de Die-Smulders, C.E.M., Tjan-Heijnen, V.C.G., Derks-Smeets, I.A.P., van Golde, R., Gomez-Garcia, E., van Osch, L.A.D.M.

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The uptake and outcome of prenatal and pre-implantation genetic diagnosis for Huntington's disease in the Netherlands (1998-2008) von van Rij, MC, de Koning Gans, PAM, van Belzen, MJ, Roos, RAC, Geraedts, JPM, De Rademaeker, M, Bijlsma, EK, de Die-Smulders, CEM

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Encephalopathic attacks in a family co-segregating myotonic dystrophy type 1, an intermediate Charcot–Marie–Tooth neuropathy and early hearing loss von Spaans, F, Faber, C G, Smeets, H J M, Hofman, P A M, Braida, C, Monckton, D G, de Die-Smulders, C E M

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