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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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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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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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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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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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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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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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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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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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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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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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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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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Saccade dysmetria in Williams–Beuren syndrome von van der Geest, J.N., Lagers-van Haselen, G.C., van Hagen, J.M., Govaerts, L.C.P., de Coo, I.F.M., de Zeeuw, C.I., Frens, M.A.

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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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Phenotype—genotype correlation in a familial/GF1R 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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Infantile Refsum disease: an inherited peroxisomal disorder: comparison with Zellweger syndrome and neonatal adrenoleukodystrophy von POLL-THE, B. T, SAUDUBRAY, J. M, WANDERS, R. J. A, SCHRAM, A. W, TAGER, J. M, OGIER, H. A. M, ODIEVRE, M, SCOTTO, J. M, MONNENS, L, GOVAERTS, L. C. P, ROELS, F, CORNELIS, A, SCHUTGENS, R. B. H

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Silver-Russell phenotype in a patient with pure trisomy 1q32.1-q42.1: further delineation of the pure 1q trisomy syndrome von van Haelst, M M, Eussen, H J F M M, Visscher, F, de Ruijter, J L M, Drop, S L S, Lindhout, D, Wouters, C H, Govaerts, L C P

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