Long-term psychological consequences of pregnancy termination for fetal abnormality: a cross-sectional study von Korenromp, M. J., Christiaens, G. C. M. L., van den Bout, J., Mulder, E. J. H., Hunfeld, J. A. M., Bilardo, C. M., Offermans, J. P. M., Visser, G. H. A.

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A prospective study on parental coping 4 months after termination of pregnancy for fetal anomalies von Korenromp, M. J., Page-Christiaens, G. C. M. L., van den Bout, J., Mulder, E. J. H., Hunfeld, J. A. M., Potters, C. M. A. A., Erwich, J. J. H. M., van Binsbergen, C. J. M., Brons, J. T. J., Beekhuis, J. R., Omtzigt, A. W. J., Visser, G. H. A.

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Improved prenatal detection of a fetal point mutation for achondroplasia by the use of size-fractionated circulatory DNA in maternal plasma-case report von Li, Y., Holzgreve, W., Page-Christiaens, G. C. M. L., Gille, J. J. P., Hahn, S.

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Detection of fetal chromosomal anomalies: does nuchal translucency measurement have added value in the era of non-invasive prenatal testing? von Lichtenbelt, K. D., Diemel, B. D. M., Koster, M. P. H., Manten, G. T. R., Siljee, J., Schuring-Blom, G. H., Page-Christiaens, G. C. M. L.

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Analysis of false-positive results of fetal RHD typing in a national screening program reveals vanishing twins as potential cause for discrepancy von Thurik, F. F., Ait Soussan, A., Bossers, B., Woortmeijer, H., Veldhuisen, B., Page-Christiaens, G. C. M. L., de Haas, M., van der Schoot, C. E.

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Rapid detection of chromosomal aneuploidies in uncultured amniocytes by multiplex ligation-dependent probe amplification (MLPA) von Hochstenbach, R., Meijer, J., van de Brug, J., Vossebeld-Hoff, I., Jansen, R., van der Luijt, R. B., Sinke, R. J., Page-Christiaens, G. C. M. L., Ploos van Amstel, J.-K., de Pater, J. M.

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Noninvasive fetal blood group genotyping of rhesus D, c, E and of K in alloimmunised pregnant women: evaluation of a 7‐year clinical experience von Scheffer, PG, van der Schoot, CE, Page‐Christiaens, GCML, de Haas, M

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Genomic futures of prenatal screening: ethical reflection von Dondorp, W.J., Page-Christiaens, G.C.M.L., de Wert, G.M.W.R

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Noninvasive fetal genotyping of human platelet antigen‐1a von Scheffer, PG, Ait Soussan, A, Verhagen, OJHM, Page‐Christiaens, GCML, Oepkes, D, de Haas, M, van der Schoot, CE

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Detection of fetal RHD-specific sequences in maternal plasma von Faas, BHW, Beuling, EA, Christiaens, GC ML, von dem Borne, AEG Kr, van der School, CE

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Earliest gestational age for fetal sexing in cell-free maternal plasma von Rijnders, R. J. P., Van Der Luijt, R. B., Peters, E. D. J., Goeree, J. K., Van Der Schoot, C. E., Ploos Van Amstel, J. K., Christiaens, G. C. M. L.

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Does 17‐α‐hydroxyprogesterone caproate affect fetal biometry and birth weight in twin pregnancy? von Mulder, E. J. H., Versteegh, E. M. J., Bloemenkamp, K. W. M., Lim, A. C., Mol, B. W. J., Bekedam, D. J., Kwee, A., Bruinse, H. W., Christiaens, G. C. M. L.

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Unexplained False Negative Results in Noninvasive Prenatal Testing: Two Cases Involving Trisomies 13 and 18 von Kusters, K., Akkermans, O., Ploos van Amstel, J. K., Schuring-Blom, G. H., van Zon, P., Manten, G. T. R., Brouwer, T., van Harssel, J. J. T., Lichtenbelt, K. D., van Oppen, A. C. C., Page-Christiaens, G. C. M. L., Hochstenbach, R., Elferink, M.

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Detection of Fetal Chromosomal Anomalies: Does Nuchal Translucency Measurement Have Added Value in the Era of Non-invasive Prenatal Testing? von Lichtenbelt, K D, Diemel, B. D M, Koster, M. P H, Manten, G. T R, Siljee, J, Schuring-Blom, G H, Page-Christiaens, G. C. M L

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Pitfalls in prenatal diagnosis: cytogenetic analysis in amniocytes fails to detect mosaic r(12) von de Pater, J. M., Scheres, J. M. J. C., Christiaens, G. C. M. L., Ausems, M. G. E. M.

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Adverse obstetric outcome in low- and high-risk pregnancies: predictive value of maternal serum screening von van Rijn, M, van Der Schouw, Y.T, Hagenaars, A.M, Visser, G.H.A, Christiaens, G.C.M.L

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Prenatal detection of complex chromosomal aberrations using advanced molecular cytogenetic techniques von de Pater, J. M., Govaerts, L. C. P., de Man, S. A., van der Sijs-Bos, C. J. M., Christiaens, G. C. M. L., van Dam, W. M., Loneus, W. H., Engelen, J. J. M.

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Antiepileptic drug regimens and major congenital abnormalities in the offspring von Samrén, E. Bettina, Van Duijn, Cornelia M., Lieve Christiaens, G. C. M., Hofman, Albert, Lindhout, Dick

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Comparative genomic hybridization for cytogenetic evaluation of stillbirth von Christiaens, G.C.M.L, Vissers, J, Poddighe, P.J, de Pater, J.M

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First-trimester septated cystic hygroma: prevalence, natural history, and pediatric outcome von Pistorius, L R, Page-Christiaens, G C M L

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