Works matching AU Van Opstal, D.

Results: 29

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

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

A participatory modelling approach to define farm-scale effects of reclaimed wastewater irrigation in the Lockyer Valley, Australia.

Published in:

Water International, 2012, v. 37, n. 7, p. 843, doi. 10.1080/02508060.2012.733673

By:

van Opstal, Jonna D.;
Huibers, Frans P.;
Cresswell, Richard G.

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

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

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

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

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

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

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

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