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Full TextIssue DateTitleAuthor(s)
2012Considering factors affecting the parental decision to abort after a prenatal diagnosis of a sex chromosome abnormality.Pieters, J.J.P.M.; Kooper, A.J.A.; Feuth, T.; Smits, A.P.T.
2012Non-targeted whole genome 250K SNP array analysis as replacement for karyotyping in fetuses with structural ultrasound anomalies: evaluation of a one-year experience.Faas, B.H.W.; Feenstra, I.; Eggink, A.J.; Kooper, A.J.A.; Pfundt, R.; Vugt, J.M.G. van; Leeuw, N. de
2011Parents' perspectives on the unforeseen finding of a fetal sex chromosomal aneuploidyPieters, J.J.; Kooper, A.J.A.; Eggink, A.J.; Verhaak, C.M.; Otten, B.J.; Braat, D.D.M.; Smits, A.P.T.; Leeuwen, E. van
2010Innovation of prenatal genetic diagnostics in relation to improvement of care.Kooper, A.J.A.
2010A small (sSMC) chromosome 22 due to a maternal translocation between chromosomes 8 and 22: a case report.Mundhofir, F.E.P.; Kooper, A.J.A.; Winarni, T.I.; Smits, A.P.T.; Faradz, S.; Hamel, B.C.J.
2010Identification of clinically significant, submicroscopic chromosome alterations and UPD in fetuses with ultrasound anomalies using genome-wide 250k SNP array analysis.Faas, B.H.W.; Burgt, C.J.A.M. van der; Kooper, A.J.A.; Pfundt, R.; Hehir, J.Y.; Smits, A.P.T.; Leeuw, N. de
2009Parent's attitudes towards full-scale prenatal testing for genetic disorders.Pieters, J.J.; Kooper, A.J.A.; Smits, A.P.T.; Vries, J. de
2009Detection of chromosome aneuploidies in chorionic villus samples by multiplex ligation-dependent probe amplification.Kooper, A.J.A.; Faas, B.H.W.; Feuth, A.B.; Creemers, J.W.T.; Zondervan, H.H.; Boekkooi, P.F.; Quartero, R.W.; Rijnders, R.J.; Burgt, C.J.A.M. van der; Geurts van Kessel, A.H.M.; Smits, A.P.T.
2008Alfafoetoprotene in vruchtwater voor de detectie van neuralebuisdefecten: beperkte meerwaarde boven de 20-weken-echo; retrospectief onderzoekKooper, A.J.A.; Smits, A.P.T.; Feuth, A.B.; Rijnders, R.J.P.
2008Alfafoetoproteïnebepaling in vruchtwater voor de detectie van neuralebuisdefecten: beperkte meerwaarde boven de 20-wekenecho; retrospectief onderzoek.Kooper, A.J.A.; Smits, A.P.T.; Feuth, A.B.; Burgt, I. van der; Zondervan, H.A.; Quartero, R.W.P.; Boekkooi, P.F.; Rijnders, R.J.P.; Creemers, J.W.T.; Thomas, C.M.G.
2008Multiplex ligation-dependent probe amplification versus karyotyping in prenatal diagnosis : the M.A.K.E. studyBoormans, E.M.; Birnie, E.; Wildschut, H.I.J.; Schuring-Blom, H.G.; Oepkes, D.; Oppen, C.A. van; Nijhuis, J.G.; Macville, M.V.E.; Kooper, A.J.A.; Huijsdens, K.; Hoffer, M.V.; Go, A.; Creemers, J.W.T.; Bhola, S.L.; Bilardo, K.M.; Suijkerbuijk, R.F.; Bouman, K.; Galjaard, R.J.; Bonsel, G.J.; Lith, J.M. van
2008Multiplex ligation-dependent probe amplification (MLPA) as a stand-alone test for rapid aneuploidy detection in amniotic fluid cells.Kooper, A.J.A.; Faas, B.H.W.; Kater-Baats, E.; Feuth, T.; Janssen, J.C.; Burgt, I. van der; Lotgering, F.K.; Geurts van Kessel, A.H.M.; Smits, A.P.T.
2008[Alpha-foetoprotein assessment in amniotic fluid for the detection of neural tube defects: limited added value beyond week 20 ultrasound; retrospective study]Kooper, A.J.A.; Smits, A.P.T.; Feuth, A.B.; Burgt, I. van der; Zondervan, H.A.; Quartero, R.W.P.; Boekkooi, P.F.; Rijnders, R.J.P.; Creemers, J.W.T.; Thomas, C.M.G.
2007Fetal anomaly scan potentially will replace routine AFAFP assays for the detection of neural tube defects.Kooper, A.J.A.; Bruijn, D. de; Ravenswaaij-Arts, C.M.A. van; Faas, B.H.W.; Creemers, J.W.T.; Thomas, C.M.G.; Smits, A.P.T.
2006Technologische vernieuwingen in de prenatale diagnostiekKooper, A.J.A.
2006Lysosomal storage diseases in non-immune hydrops fetalis pregnancies.Kooper, A.J.A.; Janssens, P.M.W.; Groot, A.N.J.A. de; Liebrand-van Sambeek, M.L.F.; Berg, C.J.M.G. van den; Tan-Sindhunata, G.B.; Berg, P.P. van den; Bijlsma, E.K.; Smits, A.P.T.; Wevers, R.A.
2004Hydrops foetalis als mogelijk gevolg van erfelijke stofwisselingsziektenJanssens, P.M.W.; Jong, J.G.N. de; Liebrand-van Sambeek, M.L.F.; Wevers, R.A.; Groot, A. de; Kooper, A.J.A.; Tan-Sindhunata, M.B.; Bijlsma, E.

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