Publications by authors named "Diane Van Opstal"

44Publications

Patient-friendly integrated first trimester screening by NIPT and fetal anomaly scan.

Authors:
Malgorzata Ilona Srebniak Maarten F C M Knapen Marieke Joosten Karin E M Diderich Sander Galjaard Diane Van Opstal

Mol Cytogenet 2021 Jan 9;14(1). Epub 2021 Jan 9.

Department of Clinical Genetics, Erasmus MC, Wytemaweg 80, 3015 CN, Rotterdam, The Netherlands.

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January 2021

The potential diagnostic yield of whole exome sequencing in pregnancies complicated by fetal ultrasound anomalies.

Authors:
Karin E M Diderich Kathleen Romijn Marieke Joosten Lutgarde C P Govaerts Marike Polak Hennie T Bruggenwirth Martina Wilke Marjon A van Slegtenhorst Yolande van Bever Alice S Brooks Grazia M S Mancini Ingrid M B H van de Laar Joan N R Kromosoeto Maarten F C M Knapen Attie T J I Go Diane Van Opstal Lies H Hoefsloot Robert-Jan H Galjaard Malgorzata I Srebniak

Acta Obstet Gynecol Scand 2020 Nov 29. Epub 2020 Nov 29.

Department of Clinical Genetics, Erasmus Medical Center, Rotterdam, the Netherlands.

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November 2020

Noninvasive prenatal testing as compared to chorionic villus sampling is more sensitive for the detection of confined placental mosaicism involving the cytotrophoblast.

Authors:
Diane Van Opstal Geerke M Eggenhuizen Marieke Joosten Karin Diderich Lutgarde Govaerts Robert-Jan Galjaard Attie Go Maarten Knapen Marjan Boter Wai Y Cheung Nicole van Koetsveld Stefanie van Veen Walter G de Valk Fernanda Jehee Femke de Vries Iris Hollink Lies Hoefsloot Malgorzata Srebniak

Prenat Diagn 2020 09 29;40(10):1338-1342. Epub 2020 Jun 29.

Department of Clinical Genetics, Erasmus Medical Center, Rotterdam, The Netherlands.

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September 2020

Nuchal translucency of 3.0-3.4 mm an indication for NIPT or microarray? Cohort analysis and literature review.

Authors:
Olav B Petersen Eric Smith Diane Van Opstal Marike Polak Maarten F C M Knapen Karin E M Diderich Caterina M Bilardo Lidia R Arends Ida Vogel Malgorzata I Srebniak

Acta Obstet Gynecol Scand 2020 06 12;99(6):765-774. Epub 2020 May 12.

Department of Clinical Genetics, Erasmus MC, Rotterdam, The Netherlands.

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June 2020

Social and medical need for whole genome high resolution NIPT.

Authors:
Malgorzata I Srebniak Maarten F C M Knapen Lutgarde C P Govaerts Marike Polak Marieke Joosten Karin E M Diderich Laura J C M van Zutven Krista A K E Prinsen Sam Riedijk Attie T J I Go Robert-Jan H Galjaard Lies H Hoefsloot Diane Van Opstal

Mol Genet Genomic Med 2020 01 1;8(1):e1062. Epub 2019 Dec 1.

Department of Clinical Genetics, Erasmus MC, Rotterdam, the Netherlands.

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January 2020

TRIDENT-2: National Implementation of Genome-wide Non-invasive Prenatal Testing as a First-Tier Screening Test in the Netherlands.

Authors:
Karuna R M van der Meij Erik A Sistermans Merryn V E Macville Servi J C Stevens Caroline J Bax Mireille N Bekker Caterina M Bilardo Elles M J Boon Marjan Boter Karin E M Diderich Christine E M de Die-Smulders Leonie K Duin Brigitte H W Faas Ilse Feenstra Monique C Haak Mariëtte J V Hoffer Nicolette S den Hollander Iris H I M Hollink Fernanda S Jehee Maarten F C M Knapen Angelique J A Kooper Irene M van Langen Klaske D Lichtenbelt Ingeborg H Linskens Merel C van Maarle Dick Oepkes Mijntje J Pieters G Heleen Schuring-Blom Esther Sikkel Birgit Sikkema-Raddatz Dominique F C M Smeets Malgorzata I Srebniak Ron F Suijkerbuijk Gita M Tan-Sindhunata A Jeanine E M van der Ven Shama L van Zelderen-Bhola Lidewij Henneman Robert-Jan H Galjaard Diane Van Opstal Marjan M Weiss

Am J Hum Genet 2019 12 7;105(6):1091-1101. Epub 2019 Nov 7.

Department of Clinical Genetics, Amsterdam UMC, Vrije Universiteit Amsterdam, 1081HV Amsterdam, the Netherlands.

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December 2019

The clinical benefit of genome-wide cfDNA testing cannot be extrapolated from CVS data.

Authors:
Erik A Sistermans Diane Van Opstal Mireille N Bekker Mark D Pertile

Genet Med 2020 03 6;22(3):657-658. Epub 2019 Nov 6.

Victorian Clinical Genetics Services, Murdoch Children's Research Institute, Melbourne, VIC, Australia.

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March 2020

Is it feasible to select fetuses for prenatal WES based on the prenatal phenotype?

Authors:
Karin Diderich Marieke Joosten Lutgarde Govaerts Diane Van Opstal Attie Go Maarten Knapen Robert-Jan Galjaard Lies Hoefsloot Malgorzata Srebniak

Prenat Diagn 2019 10 10;39(11):1039-1040. Epub 2019 Sep 10.

Department of Clinical Genetics, Erasmus Medical Center, Rotterdam, The Netherlands.

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October 2019

Placental studies elucidate discrepancies between NIPT showing a structural chromosome aberration and a differently abnormal fetal karyotype.

Authors:
Diane Van Opstal Stefanie van Veen Marieke Joosten Karin E M Diderich Lutgarde C P Govaerts Joke Polak Nicole van Koetsveld Marjan Boter Attie T J I Go Dimitri N M Papatsonis Krista Prinsen Lies H Hoefsloot Malgorzata I Srebniak

Prenat Diagn 2019 10 13;39(11):1016-1025. Epub 2019 Aug 13.

Department of Clinical Genetics, Erasmus Medical Center, Rotterdam, The Netherlands.

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October 2019

Unexpected finding of uniparental disomy mosaicism in term placentas: Is it a common feature in trisomic placentas?

Authors:
Diane Van Opstal Karin E M Diderich Marieke Joosten Lutgarde C P Govaerts Joke Polak Marjan Boter Jasper J Saris Wai Yee Cheung Stefanie van Veen Robert van de Helm Attie T J I Go Maarten F C M Knapen Dimitri N M Papatsonis Anneke Dijkman Femke de Vries Robert-Jan H Galjaard Lies H Hoefsloot Malgorzata I Srebniak

Prenat Diagn 2018 11 27;38(12):911-919. Epub 2018 Sep 27.

Department of Clinical Genetics, Erasmus Medical Center, Rotterdam, The Netherlands.

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November 2018

Is carriership of a balanced translocation or inversion an indication for non-invasive prenatal testing?

Authors:
Malgorzata I Srebniak Ida Vogel Diane Van Opstal

Expert Rev Mol Diagn 2018 06 26;18(6):477-479. Epub 2018 Apr 26.

a Department of Clinical Genetics , Erasmus Medical Center , Rotterdam , The Netherlands.

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June 2018

Mosaic maternal 10qter deletions are associated with FRA10B expansions and may cause false-positive noninvasive prenatal screening results.

Authors:
Karin Huijsdens-van Amsterdam Roy Straver Merel C van Maarle Alida C Knegt Diane Van Opstal Frank Sleutels Dominique Smeets Erik A Sistermans

Genet Med 2018 11 1;20(11):1472-1476. Epub 2018 Mar 1.

Department of Clinical Genetics, VU University Medical Center Amsterdam, Amsterdam, The Netherlands.

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November 2018

Origin and clinical relevance of chromosomal aberrations other than the common trisomies detected by genome-wide NIPS: results of the TRIDENT study.

Authors:
Diane Van Opstal Merel C van Maarle Klaske Lichtenbelt Marjan M Weiss Heleen Schuring-Blom Shama L Bhola Mariette J V Hoffer Karin Huijsdens-van Amsterdam Merryn V Macville Angelique J A Kooper Brigitte H W Faas Lutgarde Govaerts Gita M Tan-Sindhunata Nicolette den Hollander Ilse Feenstra Robert-Jan H Galjaard Dick Oepkes Stijn Ghesquiere Rutger W W Brouwer Lean Beulen Sander Bollen Martin G Elferink Roy Straver Lidewij Henneman Godelieve C Page-Christiaens Erik A Sistermans

Genet Med 2018 04 28;20(5):480-485. Epub 2017 Sep 28.

Department of Clinical Genetics, VU University Medical Center, Amsterdam, The Netherlands.

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April 2018

The influence of SNP-based chromosomal microarray and NIPT on the diagnostic yield in 10,000 fetuses with and without fetal ultrasound anomalies.

Authors:
Malgorzata I Srebniak Maarten F C M Knapen Marike Polak Marieke Joosten Karin E M Diderich Lutgarde C P Govaerts Marjan Boter Joan N R Kromosoeto Daniella Aloysia C M van Hassel Gido Huijbregts Wilfred F J van IJcken Roger Heydanus Anneke Dijkman Toon Toolenaar Femke A T de Vries Jeroen Knijnenburg Attie T J I Go Robert-Jan H Galjaard Diane Van Opstal

Hum Mutat 2017 07 30;38(7):880-888. Epub 2017 May 30.

Department of Clinical Genetics, Erasmus Medical Centre, Rotterdam, The Netherlands.

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July 2017

Prenatal diagnosis of susceptibility loci for neurodevelopmental disorders - genetic counseling and pregnancy outcome in 57 cases.

Authors:
Lutgarde Govaerts Malgorzata Srebniak Karin Diderich Marieke Joosten Sam Riedijk Maarten Knapen Attie Go Dimitri Papatsonis Katja de Graaf Toon Toolenaar Sanne van der Steen Gido Huijbregts Jeroen Knijnenburg Femke de Vries Diane Van Opstal Robert-Jan Galjaard

Prenat Diagn 2017 Jan 29;37(1):73-80. Epub 2016 Dec 29.

Department of Clinical Genetics, Erasmus Medical Center, Rotterdam, The Netherlands.

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January 2017

Trial by Dutch laboratories for evaluation of non-invasive prenatal testing. Part I-clinical impact.

Authors:
Dick Oepkes G C Lieve Page-Christiaens Caroline J Bax Mireille N Bekker Catia M Bilardo Elles M J Boon G Heleen Schuring-Blom Audrey B C Coumans Brigitte H Faas Robert-Jan H Galjaard Attie T Go Lidewij Henneman Merryn V E Macville Eva Pajkrt Ron F Suijkerbuijk Karin Huijsdens-van Amsterdam Diane Van Opstal E J Joanne Verweij Marjan M Weiss Erik A Sistermans

Prenat Diagn 2016 Dec 15;36(12):1083-1090. Epub 2016 Nov 15.

Department of Clinical Genetics, VU University Medical Center, Amsterdam, The Netherlands.

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December 2016

Enlarged NT (≥3.5 mm) in the first trimester - not all chromosome aberrations can be detected by NIPT.

Authors:
Malgorzata I Srebniak Merel C de Wit Karin E M Diderich Lutgarde C P Govaerts Marieke Joosten Maarten F C M Knapen Marnix J Bos Gerda A G Looye-Bruinsma Mieke Koningen Attie T J I Go Robert Jan H Galjaard Diane Van Opstal

Mol Cytogenet 2016 7;9(1):69. Epub 2016 Sep 7.

Department of Clinical Genetics, Erasmus Medical Center, Wytemaweg 80, 3015 CN Rotterdam, The Netherlands.

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September 2016

Copy number variations in 375 patients with oesophageal atresia and/or tracheoesophageal fistula.

Authors:
Erwin Brosens Florian Marsch Elisabeth M de Jong Hitisha P Zaveri Alina C Hilger Vera Gisela Choinitzki Alice Hölscher Per Hoffmann Stefan Herms Thomas M Boemers Benno M Ure Martin Lacher Michael Ludwig Bert H Eussen Robert M van der Helm Hannie Douben Diane Van Opstal Rene M H Wijnen H Berna Beverloo Yolande van Bever Alice S Brooks Hanneke IJsselstijn Daryl A Scott Johannes Schumacher Dick Tibboel Heiko Reutter Annelies de Klein

Eur J Hum Genet 2016 12 20;24(12):1715-1723. Epub 2016 Jul 20.

Department of Clinical Genetics, Erasmus Medical Centre - Sophia Children's Hospital, Rotterdam, The Netherlands.

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December 2016

Clinical experience of unexpected findings in prenatal array testing.

Authors:
Marieke Joosten Karin Em Diderich Diane Van Opstal Lutgarde Cp Govaerts Sam R Riedijk A Krista E Prinsen Femke At De Vries Attie Tji Go Robert-Jan H Galjaard Malgorzata I Srebniak

Biomark Med 2016 Aug 14;10(8):831-40. Epub 2016 Jul 14.

Department of Clinical Genetics, Erasmus Medical Center, Wytemaweg 80, 3015 CN Rotterdam, The Netherlands.

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August 2016

Interstitial 6q21q23 duplication - variant of variable phenotype and incomplete penetrance or benign duplication?

Authors:
Malgorzata I Srebniak Laura J C M van Zutven Florence Petit Sonia Bouquillon Ilse P J van Heel Maarten F C M Knapen Jerome M J Cornette Andreas Kremer Diane Van Opstal Karin E M Diderich

Mol Cytogenet 2016 2;9:43. Epub 2016 Jun 2.

Department of Clinical Genetics, Erasmus MC, Ee2475, Wytemaweg 80, 3015 CN Rotterdam, The Netherlands.

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June 2016

Cytogenetic confirmation of a positive NIPT result: evidence-based choice between chorionic villus sampling and amniocentesis depending on chromosome aberration.

Authors:
Diane Van Opstal Malgorzata I Srebniak

Expert Rev Mol Diagn 2016 29;16(5):513-20. Epub 2016 Feb 29.

a Department of Clinical Genetics , Erasmus Medical Center , Rotterdam , the Netherlands.

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December 2016

False Negative NIPT Results: Risk Figures for Chromosomes 13, 18 and 21 Based on Chorionic Villi Results in 5967 Cases and Literature Review.

Authors:
Diane Van Opstal Malgorzata I Srebniak Joke Polak Femke de Vries Lutgarde C P Govaerts Marieke Joosten Attie T J I Go Maarten F C M Knapen Cardi van den Berg Karin E M Diderich Robert-Jan H Galjaard

PLoS One 2016 15;11(1):e0146794. Epub 2016 Jan 15.

Department of Clinical Genetics, Erasmus Medical Center, Rotterdam, the Netherlands.

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July 2016

Prenatal SNP array testing in 1000 fetuses with ultrasound anomalies: causative, unexpected and susceptibility CNVs.

Authors:
Malgorzata I Srebniak Karin Em Diderich Marieke Joosten Lutgarde Cp Govaerts Jeroen Knijnenburg Femke At de Vries Marjan Boter Debora Lont Maarten Fcm Knapen Merel C de Wit Attie Tji Go Robert-Jan H Galjaard Diane Van Opstal

Eur J Hum Genet 2016 May 2;24(5):645-51. Epub 2015 Sep 2.

Department of Clinical Genetics, Erasmus Medical Center, Rotterdam, The Netherlands.

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May 2016

Is prenatal cytogenetic diagnosis with genomic array indicated in pregnancies at risk for a molecular or metabolic disorder?

Authors:
Malgorzata I Srebniak Lutgarde C P Govaerts Karin E M Diderich Marieke Joosten Femke A T de Vries Robert-Jan H Galjaard Diane Van Opstal

Genet Med 2016 Apr 9;18(4):307-8. Epub 2015 Jul 9.

Department of Clinical Genetics, Erasmus Medical Center, Rotterdam, The Netherlands.

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April 2016

Benefits and burdens of using a SNP array in pregnancies at increased risk for the common aneuploidies.

Authors:
Diane Van Opstal Femke de Vries Lutgarde Govaerts Marjan Boter Debora Lont Stefanie van Veen Marieke Joosten Karin Diderich Robert-Jan Galjaard Malgorzata I Srebniak

Hum Mutat 2015 Mar;36(3):319-26

Department of Clinical Genetics, Erasmus Medical Center, Rotterdam, The Netherlands.

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March 2015

The Psychological Challenges of Replacing Conventional Karyotyping with Genomic SNP Array Analysis in Prenatal Testing.

Authors:
Sam Riedijk Karin E M Diderich Sanne L van der Steen Lutgarde C P Govaerts Marieke Joosten Maarten F C M Knapen Femke A T de Vries Diane van Opstal Aad Tibben Robert-Jan H Galjaard

J Clin Med 2014 Jul 3;3(3):713-23. Epub 2014 Jul 3.

Department of Clinical Genetics, Erasmus Medical Centre, P.O. Box 2040, Rotterdam 3000 CA, The Netherlands.

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July 2014

Types of array findings detectable in cytogenetic diagnosis: a proposal for a generic classification.

Authors:
Malgorzata I Srebniak Karin E M Diderich Lutgarde C P Govaerts Marieke Joosten Sam Riedijk Robert Jan H Galjaard Diane Van Opstal

Eur J Hum Genet 2014 Jul 6;22(7):856-8. Epub 2013 Nov 6.

Department of Clinical Genetics, Erasmus Medical Center, Rotterdam, The Netherlands.

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July 2014

0.5 Mb array as a first-line prenatal cytogenetic test in cases without ultrasound abnormalities and its implementation in clinical practice.

Authors:
Malgorzata I Srebniak Lisanne Mout Diane Van Opstal Robert-Jan H Galjaard

Hum Mutat 2013 Sep 6;34(9):1298-303. Epub 2013 Jun 6.

Department of Clinical Genetics, Erasmus MC, Rotterdam 3015GE, The Netherlands.

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September 2013

Another rare prenatal case of post-zygotic mosaic trisomy 17.

Authors:
Femke A T de Vries Lutgarde C P Govaerts Jeroen Knijnenburg Maarten F C M Knapen Grétel G Oudesluijs Debora Lont Petra Noomen Katja de Graaff Malgorzata I Srebniak Diane Van Opstal

Am J Med Genet A 2013 May 20;161A(5):1196-9. Epub 2013 Mar 20.

Department of Clinical Genetics, Erasmus MC, Rotterdam, The Netherlands.

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May 2013

Phenotypic variability of atypical 22q11.2 deletions not including TBX1.

Authors:
Judith M A Verhagen Karin E M Diderich Grétel Oudesluijs Grazia M S Mancini Alex J Eggink Anna C Verkleij-Hagoort Irene A L Groenenberg Patrick J Willems Frederik A du Plessis Stella A de Man Malgorzata I Srebniak Diane van Opstal Lorette O M Hulsman Laura J C M van Zutven Marja W Wessels

Am J Med Genet A 2012 Oct 14;158A(10):2412-20. Epub 2012 Aug 14.

Department of Clinical Genetics, Erasmus Medical Center, Rotterdam, The Netherlands.

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October 2012

Genomic SNP array as a gold standard for prenatal diagnosis of foetal ultrasound abnormalities.

Authors:
Malgorzata I Srebniak Marjan Boter Gretel O Oudesluijs Titia Cohen-Overbeek Lutgarde Cp Govaerts Karin Em Diderich Renske Oegema Maarten Fcm Knapen Ingrid Mbh van de Laar Marieke Joosten Diane Van Opstal Robert-Jan H Galjaard

Mol Cytogenet 2012 Mar 13;5(1):14. Epub 2012 Mar 13.

Department of Clinical Genetics, Erasmus MC, Rotterdam, the Netherlands.

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March 2012

Prenatally diagnosed submicroscopic familial aberrations at 18p11.32 without phenotypic effect.

Authors:
Malgorzata I Srebniak Marjan Boter Carla Ma Verboven-Peerden Gerda Ag Looye-Bruinsma Gretel Oudesluijs Robert-Jan H Galjaard Diane Van Opstal

Mol Cytogenet 2011 Dec 2;4(1):27. Epub 2011 Dec 2.

Department of Clinical Genetics, Erasmus Medical Center, Rotterdam, Dr Molewaterplein 50, 3015 GE, the Netherlands.

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December 2011

Prenatal diagnosis of alobar holoprosencephaly, cyclopia, proboscis, and isochromosome 18q in the second trimester.

Authors:
Meike Bangma Simone Lunshof Diane Van Opstal Robert J Galjaard Dimitri N M Papatsonis

AJP Rep 2011 Dec 8;1(2):73-6. Epub 2011 Jun 8.

Department of Obstetrics and Gynecology, Amphia Hospital Breda, Breda.

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December 2011

Application of SNP array for rapid prenatal diagnosis: implementation, genetic counselling and diagnostic flow.

Authors:
Malgorzata Srebniak Marjan Boter Grétel Oudesluijs Marieke Joosten Lutgarde Govaerts Diane Van Opstal Robert-Jan H Galjaard

Eur J Hum Genet 2011 Dec 22;19(12):1230-7. Epub 2011 Jun 22.

Department of Clinical Genetics, Erasmus Medical Center, Dr Molewaterplein 50, Rotterdam, The Netherlands.

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December 2011

Multiplex ligation dependent probe amplification (MLPA) for rapid distinction between unique sequence positive and negative marker chromosomes in prenatal diagnosis.

Authors:
Diane Van Opstal Marjan Boter Petra Noomen Malgorzata Srebniak Guus Hamers Robert-Jan H Galjaard

Mol Cytogenet 2011 Jan 14;4. Epub 2011 Jan 14.

Department of Clinical Genetics, Erasmus Medical Centre, PO Box 2040, 3000 CA Rotterdam, The Netherlands.

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January 2011

The fate of the mosaic embryo: chromosomal constitution and development of Day 4, 5 and 8 human embryos.

Authors:
Margarida Avo Santos Gijs Teklenburg Nick S Macklon Diane Van Opstal G Heleen Schuring-Blom Pieter-Jaap Krijtenburg Johanna de Vreeden-Elbertse Bart C Fauser Esther B Baart

Hum Reprod 2010 Aug 2;25(8):1916-26. Epub 2010 Jun 2.

Department of Reproductive Medicine and Gynaecology, University Medical Centre, Utrecht, The Netherlands.

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August 2010

The use of comparative genomic hybridization and fluorescent in situ hybridization in postmortem pathology investigation of congenital malformations.

Authors:
Natascha Goemaere Hannie Douben Diane Van Opstal Cokkie Wouters Dick Tibboel Ronald de Krijger Annelies de Klein

Pediatr Dev Pathol 2010 Mar-Apr;13(2):85-94

Department of Pathology, Erasmus MC-University Medical Center, Rotterdam, The Netherlands.

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June 2010

Interstitial 11q deletion derived from a maternal ins(4;11)(p14;q24.2q25): a patient report and review.

Authors:
Laura J C M Van Zutven Yolande van Bever Carolien C M Van Nieuwland Gido C M Huijbregts Diane Van Opstal Anne R M von Bergh Linda J A Corel Dick Tibboel Cokkie H Wouters Pino J Poddighe

Am J Med Genet A 2009 Jul;149A(7):1468-75

Department of Clinical Genetics, Erasmus MC, Rotterdam, The Netherlands.

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July 2009

An incomplete trisomy 3 rescue resulting in a marker chromosome and UPD(3)--difficulties in interpretation.

Authors:
Malgorzata Srebniak Petra Noomen Pedro dos Santos Dicky Halley Raoul van de Graaf Lutgarde Govaerts Cokkie Wouters Robert-Jan Galjaard Diane Van Opstal

Prenat Diagn 2008 Oct;28(10):967-70

Department of Clinical Genetics, Erasmus MC, Rotterdam, The Netherlands.

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October 2008

Rapid aneuploidy detection with multiplex ligation-dependent probe amplification: a prospective study of 4000 amniotic fluid samples.

Authors:
Diane Van Opstal Marjan Boter Danielle de Jong Cardi van den Berg Hennie T Brüggenwirth Hajo I J Wildschut Annelies de Klein Robert-Jan H Galjaard

Eur J Hum Genet 2009 Jan 10;17(1):112-21. Epub 2008 Sep 10.

Department of Clinical Genetics, Erasmus Medical Center, Rotterdam, The Netherlands.

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January 2009

Milder ovarian stimulation for in-vitro fertilization reduces aneuploidy in the human preimplantation embryo: a randomized controlled trial.

Authors:
Esther B Baart Elena Martini Marinus J Eijkemans Diane Van Opstal Nicole G M Beckers Arie Verhoeff Nicolas S Macklon Bart C J M Fauser

Hum Reprod 2007 Apr 4;22(4):980-8. Epub 2007 Jan 4.

Department of Reproductive Medicine and Gynaecology, University Medical Center, Utrecht, The Netherlands.

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April 2007

A familial inverted duplication 2q33-q34 identified and delineated by multiple cytogenetic techniques.

Authors:
Bert H Eussen Ingrid van de Laar Hannie Douben Leo van Kempen Ron Hochstenbach Stella A De Man Diane Van Opstal Annelies de Klein Pino J Poddighe

Eur J Med Genet 2007 Mar-Apr;50(2):112-9. Epub 2006 Nov 3.

Department of Clinical Genetics, Erasmus MC, Rotterdam, The Netherlands.

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May 2007

(Potential) false-negative diagnoses in chorionic villi and a review of the literature.

Authors:
Cardi van den Berg Diane Van Opstal Joke Polak-Knook Robert Jan Galjaard

Prenat Diagn 2006 May;26(5):401-8

Department of Clinical Genetics, Erasmus Medical Center, 3000 DR Rotterdam, The Netherlands.

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May 2006

The development of cytogenetically normal, abnormal and mosaic embryos: a theoretical model.

Authors:
Frans J Los Diane Van Opstal Cardi van den Berg

Hum Reprod Update 2004 Jan-Feb;10(1):79-94

Department of Clinical Genetics, Erasmus Medical Centre. P.O.Box 1738, NL-3000 DR Rotterdam, The Netherlands.

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September 2004