Works by Van Opstal, D.

Results: 28

Frequency of submicroscopic chromosomal aberrations in pregnancies without increased risk for structural chromosomal aberrations: systematic review and meta-analysis.
Published in:
2018
By:
- Srebniak, M. I.;
- Joosten, M.;
- van Veen, S.;
- Van Opstal, D.;
- Go, A. T. J. I.;
- Knapen, M. F. C. M.;
- Polak, M.;
- Arends, L. R.
Publication type:
journal article
P16.04: Prevalence of submicroscopic chromosome aberrations in pregnancies without increased risk for structural chromosome aberrations: a systematic review of the literature.
Published in:
Ultrasound in Obstetrics & Gynecology, 2017, v. 50, p. 205, doi. 10.1002/uog.18158
By:
- Srebniak, M.I.;
- Joosten, M.;
- Knapen, M.;
- Arends, L.;
- Polak, M.;
- Van Veen, S.;
- Go, A.;
- Van Opstal, D.
Publication type:
Article
P16.05: The influence of chromosomal microarray and NIPT on the diagnostic yield in 6,811 high-risk pregnancies without ultrasound anomalies.
Published in:
Ultrasound in Obstetrics & Gynecology, 2017, v. 50, p. 206, doi. 10.1002/uog.18159
By:
- 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.
Publication type:
Article
EP06.03: Be aware of a diagnostic delay: Rotterdam's experience with NIPT in 1071 high-risk pregnancies.
Published in:
Ultrasound in Obstetrics & Gynecology, 2017, v. 50, p. 284, doi. 10.1002/uog.18407
By:
- Diderich, K.E.;
- Srebniak, M.I.;
- Knapen, M.;
- Joosten, M.;
- Govaerts, L.;
- Ijcken, W.F.;
- Go, A.;
- Galjaard, R.J.;
- Van Opstal, D.
Publication type:
Article
Prenatal and postnatal findings in small-for-gestational-age fetuses without structural ultrasound anomalies at 18-24 weeks.
Published in:
2017
By:
- 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.
Publication type:
journal article
Whole-genome array as a first-line cytogenetic test in prenatal diagnosis.
Published in:
Ultrasound in Obstetrics & Gynecology, 2015, v. 45, n. 4, p. 363, doi. 10.1002/uog.14745
By:
- 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.
Publication type:
Article
Abnormal non-invasive prenatal test results concordant with karyotype of cytotrophoblast but not reflecting abnormal fetal karyotype.
Published in:
Ultrasound in Obstetrics & Gynecology, 2014, v. 44, n. 1, p. 109, doi. 10.1002/uog.13334
By:
- Srebniak, M. I.;
- Diderich, K. E. M.;
- Noomen, P.;
- Dijkman, A.;
- de Vries, F. A. T.;
- van Opstal, D.
Publication type:
Article
Additional value of prenatal genomic array testing in fetuses with isolated structural ultrasound abnormalities and a normal karyotype: a systematic review of the literature.
Published in:
Ultrasound in Obstetrics & Gynecology, 2014, v. 43, n. 2, p. 139, doi. 10.1002/uog.12575
By:
- de wit, M. C.;
- Srebniak, M. I.;
- Govaerts, L. C. P.;
- Van Opstal, D.;
- Galjaard, R. J. H.;
- Go, A. T. J. I.
Publication type:
Article
Screening for aneuploidies of ten different chromosomes in two rounds of FISH: a short and reliable protocol.
Published in:
Prenatal Diagnosis, 2004, v. 24, n. 12, p. 955, doi. 10.1002/pd.1052
By:
- Baart, E. B.;
- Martini, E.;
- Van Opstal, D.
Publication type:
Article
Management of prenatally detected trisomy 8 mosaicism.
Published in:
Prenatal Diagnosis, 2001, v. 21, n. 12, p. 1075, doi. 10.1002/pd.215
By:
- van Haelst, M. M.;
- Van Opstal, D.;
- Lindhout, D.;
- Los, F. J.
Publication type:
Article
False-negative findings in chorionic villi.
Published in:
1999
By:
- Los, Frans J.;
- Van Opstal, Diane;
- Los, F J;
- Van Opstal, D
Publication type:
commentary
Full monosomy 21, prenatally diagnosed by fluorescent in situ hybridization.
Published in:
1997
By:
- JOOSTEN, ANNE M. S.;
- DE VOS, SANDRA;
- VAN OPSTAL, DIANE;
- BRANDENBURG, HELEN;
- GAILLARD, JOHANNES L. J.;
- VERMEIJ-KEERS, CHRISTL;
- Joosten, A M;
- De Vos, S;
- Van Opstal, D;
- Brandenburg, H;
- Gaillard, J L;
- Vermeij-Keers, C
Publication type:
journal article
Prenatal diagnosis of mosaic tetrasomy 12p/trisomy 12p by fluorescent in situ hybridization in amniotic fluid cells: a case report of Pallister-Killian syndrome.
Published in:
1995
By:
- Los, F J;
- Van Opstal, D;
- Schol, M P;
- Gaillard, J L;
- Brandenburg, H;
- Van Den Ouweland, A M;
- in 't Veld, P A
Publication type:
journal article
Increased incidence of cytogenetic abnormalities in chorionic villus samples from pregnancies established by in vitro fertilization and embryo transfer (IVF-ET).
Published in:
Prenatal Diagnosis, 1995, v. 15, n. 10, p. 975, doi. 10.1002/pd.1970151014
By:
- Veld, P. A. In't;
- van Opstal, D.;
- van den Berg, C.;
- van Ooijen, M.;
- Brandenburg, H.;
- Pijpers, L.;
- Jahoda, M. G. J.;
- Stijnen, Th.;
- Los, F. J.
Publication type:
Article
Retrospective study of trisomy 18 in chorionic villi with fluorescent in situ hybridization on archival direct preparations.
Published in:
1995
By:
- van Opstal, Diane;
- van den Berg, Cardi;
- Jahoda, Milena G. J.;
- Brandenburg, Helen;
- Los, Frans J.;
- Veld, Peter A. In'T;
- Van Opstal, D;
- van den Berg, C;
- Jahoda, M G;
- Brandenburg, H;
- Los, F J
Publication type:
journal article
Application of fluorescent in situ hybridization for 'de novo' anomalies in prenatal diagnosis.
Published in:
1993
By:
- Van Opstal, D.;
- Eussen, H. J.;
- Van Hemel, J. O.;
- Sachs, E. S.
Publication type:
journal article
Pregnant couples at increased risk for common aneuploidies choose maximal information from invasive genetic testing.
Published in:
Clinical Genetics, 2015, v. 88, n. 1, p. 25, doi. 10.1111/cge.12479
By:
- 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.
Publication type:
Article
Choosing between Higher and Lower Resolution Microarrays: do Pregnant Women Have Sufficient Knowledge to Make Informed Choices Consistent with their Attitude?
Published in:
Journal of Genetic Counseling, 2018, v. 27, n. 1, p. 85, doi. 10.1007/s10897-017-0124-5
By:
- 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.
Publication type:
Article
SNP array detects chromosome aberrations that we thought do not exist: the first case of an isochromosome Xp (i(X)(p10))
Published in:
2014
By:
- Srebniak, M I;
- Bos, M J;
- de Vries, F A T;
- Heydanus, R;
- Wessels, M W;
- Van Opstal, D
Publication type:
Journal Article
SNP array detects chromosome aberrations that we thought do not exist: the first case of an isochromosome Xp (i(X)(p10)).
Published in:
2014
By:
- Srebniak, M. I.;
- Bos, M. J.;
- Vries, F. A. T.;
- Heydanus, R.;
- Wessels, M. W.;
- Van Opstal, D.
Publication type:
Other
An incomplete trisomy 3 rescue resulting in a marker chromosome and UPD(3)--difficulties in interpretation.
Published in:
2008
By:
- Srebniak M;
- Noomen P;
- dos Santos P;
- Halley D;
- van de Graaf R;
- Govaerts L;
- Wouters C;
- Galjaard RJ;
- Van Opstal D
Publication type:
Journal Article
False positive FISH diagnosis of monosomy X in uncultured amniotic fluid cells due to a chromosome Y deletion.
Published in:
Prenatal Diagnosis, 2008, v. 28, n. 9, p. 871, doi. 10.1002/pd.2055
By:
- Wilmink, F. A.;
- Van Opstal, D.;
- Papatsonis, D. N. M.;
- Galjaard, R. J. H.
Publication type:
Article
FISH analysis of 15 chromosomes in human day 4 and 5 preimplantation embryos: the added value of extended aneuploidy detection.
Published in:
Prenatal Diagnosis, 2007, v. 27, n. 1, p. 55, doi. 10.1002/pd.1623
By:
- Baart, E. B.;
- van den Berg, I.;
- Martini, E.;
- Eussen, H. J.;
- Fauser, B. C. J. M.;
- Opstal, D. Van
Publication type:
Article
Prevalence of tetraploid metaphases in semidirect and cultured chorionic villi.
Published in:
2001
By:
- Noomen, Petra;
- van den Berg, Cardi;
- de Ruyter, Jacqueline L.M.;
- Van Opstal, Diane;
- Los, Frans J.;
- Noomen, P;
- van den Berg, C;
- de Ruyter, J L;
- Van Opstal, D;
- Los, F J
Publication type:
journal article
Determination of the parent of origin in nine cases of prenatally detected chromosome aberrations found after intracytoplasmic sperm injection.
Published in:
Human Reproduction, 1997, v. 12, n. 4, p. 682, doi. 10.1093/humrep/12.4.682
By:
- Van Opstal, D;
- Los, F J;
- Ramlakhan, S;
- Van Hemel, J O;
- Van Den Ouweland, A M;
- Brandenburg, H;
- Pieters, M H;
- Verhoeff, A;
- Vermeer, M C;
- Dhont, M;
- In't Veld, P A
Publication type:
Article
Does confined placental mosaicism account for adverse perinatal outcomes in IVF pregnancies?
Published in:
Human Reproduction, 2008, v. 23, n. 5, p. 1107
By:
- B.C. Jacod;
- K.D. Lichtenbelt;
- G.H. Schuring-Blom;
- J.S.E. Laven;
- D. van Opstal;
- M.J.C. Eijkemans;
- N.S. Macklon;
- on behalf of the IVF-CPM Study Group
Publication type:
Article
Preimplantation genetic screening reveals a high incidence of aneuploidy and mosaicism in embryos from young women undergoing IVF.
Published in:
Human Reproduction, 2006, v. 21, n. 1, p. 223, doi. 10.1093/humrep/dei291
By:
- E.B. Baart;
- E. Martini;
- I. van den Berg;
- N.S. Macklon;
- R-J.H. Galjaard;
- B.C.J.M. Fauser;
- D. Van Opstal
Publication type:
Article
Fluorescence in situ hybridization analysis of two blastomeres from day 3 frozen–thawed embryos followed by analysis of the remaining embryo on day 5.
Published in:
Human Reproduction, 2004, v. 19, n. 3, p. 685, doi. 10.1093/humrep/deh094
By:
- Baart, E. B.;
- Opstal, D. Van;
- Los, F. J.;
- Fauser, B. C. J. M.;
- Martini, E.
Publication type:
Article