D. Opstal

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Benefits and Burdens of Using a SNP Array in Pregnancies at Increased Risk for the Common Aneuploidies

R. Galjaard, M. Srebniak, M. Joosten, 2015, Human mutation.

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

M. Knapen, J. Knijnenburg, R. Galjaard, 2015, European Journal of Human Genetics.

FISH analysis of 15 chromosomes in human day 4 and 5 preimplantation embryos: the added value of extended aneuploidy detection

B. Fauser, D. Opstal, E. Baart, 2007, Prenatal diagnosis.

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

R. Galjaard, M. Srebniak, M. Joosten, 2011, European Journal of Human Genetics.

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

R. Galjaard, M. Srebniak, M. Joosten, 2013, European Journal of Human Genetics.

Chapter 4 Mosaic maternal 10 qter deletions are associated with FRA 10 B expansions and may cause false positive NIPT results

D. Smeets, E. Sistermans, F. Sleutels, 2018 .

Molecular cytogenetics in prenatal diagnosis

D. Opstal, 1998 .

Prenatal Diagnosis of Alobar Holoprosencephaly, Cyclopia, Proboscis, and Isochromosome 18q in the Second Trimester

D. Papatsonis, R. Galjaard, D. Opstal, 2011, American Journal of Perinatology Reports.

Prenatal detection of trisomy 18 caused by isochromosome 18p and 18q formation.

D. Opstal, F. Los, C. van den Berg, 1999, American journal of medical genetics.

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

D. Jong, A. Klein, R. Galjaard, 2009, European Journal of Human Genetics.

Interstitial 11 q Deletion Derived From a Maternal ins ( 4 ; 11 ) ( p 14 ; q 24 . 2 q 25 ) : A Patient Report and Review

D. Tibboel, L. Zutven, Y. Bever, 2009 .

Does confined placental mosaicism account for adverse perinatal outcomes in IVF pregnancies?

M. Eijkemans, J. Laven, K. Lichtenbelt, 2008, Human reproduction.

Screening for aneuploidies of ten different chromosomes in two rounds of FISH: a short and reliable protocol

D. Van Opstal, D. Opstal, E. Baart, 2004, Prenatal diagnosis.

Management of prenatally detected trisomy 8 mosaicism

D. Lindhout, M. Haelst, D. Van Opstal, 2001, Prenatal diagnosis.

Case of 45,X/46,XY mosaicism with non-mosaic discordance between short-term villi (45,X) and cultured villi (46,XY).

D. Van Opstal, D. Opstal, H. Brandenburg, 2000, American journal of medical genetics.

Nasopharyngeal teratoma and mosaic tetrasomy 1q detected at amniocentesis. A case report and review of the literature.

M. Baaij, J. Lind, G. Beverstock, 1999, Cancer genetics and cytogenetics.

Preimplantation genetic screening reveals a high incidence of aneuploidy and mosaicism in embryos from young women undergoing IVF.

B. Fauser, R. Galjaard, D. Van Opstal, 2006, Human reproduction.

Whole‐genome array as a first‐line cytogenetic test in prenatal diagnosis

M. Knapen, F. D. de Vries, R. Galjaard, 2015, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Prenatal and postnatal findings in small‐for‐gestational‐age fetuses without structural ultrasound anomalies at 18–24 weeks

D. Papatsonis, M. Knapen, F. D. de Vries, 2017, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

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

M. Knapen, J. Knijnenburg, R. Galjaard, 2015, European Journal of Human Genetics.

Ring chromosome 18 in a fetus with only facial anomalies.

J. Kros, D. Van Opstal, D. Opstal, 1996, American journal of medical genetics.

Determination of the parent of origin in nine cases of prenatally detected chromosome aberrations found after intracytoplasmic sperm injection.

A. V. D. van den Ouweland, P. in’t Veld, S. Ramlakhan, 1997, Human reproduction.

Frequency of submicroscopic chromosomal aberrations in pregnancies without increased risk for structural chromosomal aberrations: systematic review and meta‐analysis

L. Arends, M. Knapen, M. Srebniak, 2017, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.