First trimester anomaly scan using virtual reality (VR FETUS study): study protocol for a randomized clinical trial
Pietersma, C. S., Mulders, A. G. M. G. J., Moolenaar, L. M., Hunink, M. G. M., Koning, A. H. J., Willemsen, S. P., Go, A. T. J. I., Steegers, E. A. P., Rousian, M.
Published in BMC pregnancy and childbirth (07.09.2020)
Published in BMC pregnancy and childbirth (07.09.2020)
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Frequency of submicroscopic chromosomal aberrations in pregnancies without increased risk for structural chromosomal aberrations: systematic review and meta‐analysis
Srebniak, M. I., Joosten, M., Knapen, M. F. C. M., Arends, L. R., Polak, M., van Veen, S., Go, A. T. J. I., Van Opstal, D.
Published in Ultrasound in obstetrics & gynecology (01.04.2018)
Published in Ultrasound in obstetrics & gynecology (01.04.2018)
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Prenatal and postnatal findings in small‐for‐gestational‐age fetuses without structural ultrasound anomalies at 18–24 weeks
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.
Published in Ultrasound in obstetrics & gynecology (01.03.2017)
Published in Ultrasound in obstetrics & gynecology (01.03.2017)
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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?
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.
Published in Journal of genetic counseling (01.02.2018)
Published in Journal of genetic counseling (01.02.2018)
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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
de wit, M. C., Srebniak, M. I., Govaerts, L. C. P., Van Opstal, D., Galjaard, R. J. H., Go, A. T. J. I.
Published in Ultrasound in obstetrics & gynecology (01.02.2014)
Published in Ultrasound in obstetrics & gynecology (01.02.2014)
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Confined placental mosaicism: Distribution of chromosomally abnormal cells over the term placenta
Eggenhuizen, G.M., van Veen, S., van Koetsveld, N., Go, A.T.J.I., Diderich, K.E.M., Joosten, M., van den Born, M., Srebniak, M.I., Van Opstal, D.
Published in Placenta (Eastbourne) (02.09.2024)
Published in Placenta (Eastbourne) (02.09.2024)
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Advanced genomic testing may aid in counseling of isolated agenesis of the corpus callosum on prenatal ultrasound
Wit, M.C., Boekhorst, F., Mancini, G.M., Smit, L.S., Groenenberg, I.A.L., Dudink, J., Vries, F.A.T., Go, A.T.J.I., Galjaard, R.J.H.
Published in Prenatal diagnosis (01.12.2017)
Published in Prenatal diagnosis (01.12.2017)
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Whole‐genome array as a first‐line cytogenetic test in prenatal diagnosis
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.
Published in Ultrasound in obstetrics & gynecology (01.04.2015)
Published in Ultrasound in obstetrics & gynecology (01.04.2015)
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Amniocentesis is still the best option for advanced genomic testing in case of fetal malformations
Wit, M.C., Bunnik, E.M., Go, A.T.J.I., Beaufort, I.D., Hofstra, R.M.W., Steegers, E.A.P., Galjaard, R.J.H.
Published in Prenatal diagnosis (01.12.2017)
Published in Prenatal diagnosis (01.12.2017)
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Perinatal mortality and mode of delivery in monochorionic diamniotic twin pregnancies ≥32 weeks of gestation: a multicentre retrospective cohort study
Hack, KEA, Derks, JB, Elias, SG, van Mameren, FA, Koopman‐Esseboom, C, Mol, BWJ, Lopriore, E, Schaap, AHP, Arabin, B, Duvekot, JJ, Go, ATJI, Wieselmann, E, Eggink, AJ, Willekes, C, Vandenbussche, FPHA, Visser, GHA
Published in BJOG : an international journal of obstetrics and gynaecology (01.08.2011)
Published in BJOG : an international journal of obstetrics and gynaecology (01.08.2011)
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C21ORF105, A chromosome 21-encoded mRNA, is not a discriminative marker gene for prediction of Down syndrome in maternal plasma
Go, A. T. J. I., Visser, A., Mulders, M. A. M., Twisk, J. W. R., Blankenstein, M. A., van Vugt, J. M. G., Oudejans, C. B. M.
Published in Prenatal diagnosis (01.02.2007)
Published in Prenatal diagnosis (01.02.2007)
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Non-invasive prenatal assessment of trisomy 21 by multiplexed maternal plasma DNA sequencing: large scale validity study
Chiu, Rossa W K, Akolekar, Ranjit, Zheng, Yama W L, Leung, Tak Y, Sun, Hao, Chan, K C Allen, Lun, Fiona M F, Go, Attie T J I, Lau, Elizabeth T, To, William W K, Leung, Wing C, Tang, Rebecca Y K, Au-Yeung, Sidney K C, Lam, Helena, Kung, Yu Y, Zhang, Xiuqing, van Vugt, John M G, Minekawa, Ryoko, Tang, Mary H Y, Wang, Jun, Oudejans, Cees B M, Lau, Tze K, Nicolaides, Kypros H, Lo, Y M Dennis
Published in BMJ (11.01.2011)
Published in BMJ (11.01.2011)
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Evaluation of a programme for the prenatal screening for Down's syndrome by ultrasonographic nuchal translucency measurement and serum determinations in the first trimester of pregnancy
Go, A T J I, Hupkes, H W Dikker, Lomecky, M, Twisk, J, Blankenstein, J M, van Vugt, J M G
Published in Nederlands tijdschrift voor geneeskunde (10.12.2005)
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Published in Nederlands tijdschrift voor geneeskunde (10.12.2005)
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C210RF105, A chromosome 21-encoded mRNA, is not a discriminative marker gene for prediction of down syndrome in maternal plasma
GO, A. T. J. I, VISSER, A, MULDERS, M. A. M, TWISK, J. W. R, BLANKENSTEIN, M. A, VAN VUGT, J. M. G, OUDEJANS, C. B. M
Published in Prenatal diagnosis (2007)
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Published in Prenatal diagnosis (2007)
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Ultrafast Scan Magnetic Resonance in Prenatal Diagnosis
Wagenvoort, A.M., Bekker, M.N., Go, A.T.J.I., Vandenbussche, F.P.H.A., van Buchem, M.A., Valk, J., van Vugt, J.M.G.
Published in Fetal diagnosis and therapy (01.11.2000)
Published in Fetal diagnosis and therapy (01.11.2000)
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