Additional value of prenatal genomic array testing in fetuses with isolated structural ultrasound abnormalities and a normal karyotype: a systematic review of the literature von de wit, M. C., Srebniak, M. I., Govaerts, L. C. P., Van Opstal, D., Galjaard, R. J. H., Go, A. T. J. I.

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The Psychological Impact of Prenatal Diagnosis and Disclosure of Susceptibility Loci: First Impressions of Parents’ Experiences von van der Steen, S. L., Riedijk, S. R., Verhagen-Visser, J., Govaerts, L. C. P., Srebniak, M. I., Van Opstal, D., Joosten, M., Knapen, M. F. C. M., Tibben, A., Diderich, K. E. M., Galjaard, R. J. H.

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Pregnant couples at increased risk for common aneuploidies choose maximal information from invasive genetic testing von van der Steen, S.L., Diderich, K.E.M., Riedijk, S.R., Verhagen-Visser, J., Govaerts, L.C.P., Joosten, M., Knapen, M.F.C.M., Van Opstal, D., Srebniak, M.I., Tibben, A., Galjaard, R.J.H.

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Prenatal and postnatal findings in small‐for‐gestational‐age fetuses without structural ultrasound anomalies at 18–24 weeks von de Wit, M. C., Srebniak, M. I., Joosten, M., Govaerts, L. C. P., Kornelisse, R. F., Papatsonis, D. N. M., de Graaff, K., Knapen, M. F. C. M., Bruggenwirth, H. T., de Vries, F. A. T., Van Veen, S., Van Opstal, D., Galjaard, R. J. H., Go, A. T. J. I.

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Whole‐genome array as a first‐line cytogenetic test in prenatal diagnosis von Srebniak, M. I., Van Opstal, D., Joosten, M., Diderich, K. E. M., de Vries, F. A. T., Riedijk, S., Knapen, M. F. C. M., Go, A. T. J. I., Govaerts, L. C. P., Galjaard, R.‐J. H.

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Genetic risk factors in infertile men with severe oligozoospermia and azoospermia von Dohle, G.R., Halley, D.J.J., Van Hemel, J.O., van den Ouwel, A.M.W., Pieters, M.H.E.C., Weber, R.F.A., Govaerts, L.C.P.

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Omphalocele: comparison of outcome following prenatal or postnatal diagnosis von Cohen‐Overbeek, T. E., Tong, W. H., Hatzmann, T. R., Wilms, J. F., Govaerts, L. C. P., Galjaard, R. J. H., Steegers, E. A. P., Hop, W. C. J., Wladimiroff, J. W., Tibboel, D.

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Outcome of pregnancies complicated by oligohydramnios or anhydramnios of renal origin von Grijseels, E. W. M., van-Hornstra, PTM Echteld, Govaerts, L. C. P., Cohen-Overbeek, T. E., de Krijger, R. R., Smit, B. J., Cransberg, K.

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Choosing between Higher and Lower Resolution Microarrays: do Pregnant Women Have Sufficient Knowledge to Make Informed Choices Consistent with their Attitude? von van der Steen, S. L., Bunnik, E. M., Polak, M. G., Diderich, K. E. M., Verhagen-Visser, J., Govaerts, L. C. P., Joosten, M., Knapen, M. F. C. M., Go, A. T. J. I., Van Opstal, D., Srebniak, M. I., Galjaard, R. J. H., Tibben, A., Riedijk, S. R.

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Phenotype–genotype correlation in a familial IGF1R microdeletion case von Veenma, D C M, Eussen, H J, Govaerts, L C P, de Kort, S W K, Odink, R J, Wouters, C H, Hokken-Koelega, A C S, de Klein, A

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EP06.03: Be aware of a diagnostic delay: Rotterdam's experience with NIPT in 1071 high‐risk pregnancies von Diderich, K.E., Srebniak, M.I., Knapen, M., Joosten, M., Govaerts, L., Ijcken, W.F., Go, A., Galjaard, R.J., Van Opstal, D.

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P16.05: The influence of chromosomal microarray and NIPT on the diagnostic yield in 6,811 high‐risk pregnancies without ultrasound anomalies von Srebniak, M.I., Knapen, M., Polak, M., Joosten, M., Diderich, K.E., Govaerts, L., Ijcken, W.F., Heydanus, R., Dijkman, A., Toolenaar, T., de Vries, F.A., Knijnenburg, J., Go, A., Galjaard, R.J., Van Opstal, D.

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Contribution of CYLN2 and GTF2IRD1 to neurological and cognitive symptoms in Williams Syndrome von van Hagen, J.M, van der Geest, J.N, van der Giessen, R.S, Lagers-van Haselen, G.C, Eussen, H.J.F.M.M, Gille, J.J.P, Govaerts, L.C.P, Wouters, C.H, de Coo, I.F.M, Hoogenraad, C.C, Koekkoek, S.K.E, Frens, M.A, van Camp, N, van der Linden, A, Jansweijer, M.C.E, Thorgeirsson, S.S, De Zeeuw, C.I

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Visual depth processing in Williams-Beuren syndrome von VAN DER GEEST, J. N, LAGERS-VAN HASELEN, G. C, VAN HAGEN, J. M, BRENNER, E, GOVAERTS, L. C. P, DE COO, I. F. M, FRENS, M. A

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268 Short-term pulmonary rehabilitation program in children and adolescents with chronic respiratory disease von Van de Wijdeven, P, Govaerts, L, Spooren, K, Van Aerschot, K, Moens, M

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Facial and pituitary morphology are related in Dutch patients with GH deficiency von De Graaff, L. C. G., Baan, J., Govaerts, L. C. P., Hokken-Koelega, A. C. S.

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Acute intramural haematoma of the ascending aorta von Govaerts, L., Withofs, N., Durieux, R., Spote, V., Hustinx, R.

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Savings and extinction of conditioned eyeblink responses in fragile X syndrome von Smit, A. E., Van Der Geest, J. N., Vellema, M., Koekkoek, S. K. E., Willemsen, R., Govaerts, L. C. P., Oostra, B. A., De Zeeuw, C. I., VanderWerf, F.

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Exceptional good cognitive and phenotypic profile in a male carrying a mosaic mutation in the FMR1 gene von Govaerts, LCP, Smit, AE, Saris, JJ, VanderWerf, F, Willemsen, R, Bakker, CE, De Zeeuw, CI, Oostra, BA

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A genome-wide linkage scan in a Dutch family identifies a premature ovarian failure susceptibility locus von Oldenburg, R.A., van Dooren, M.F., de Graaf, B., Simons, E., Govaerts, L., Swagemakers, S., Verkerk, J.M.H., Oostra, B.A., Bertoli-Avella, A.M.

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