1. 0.5 Mb Array as a First‐Line Prenatal Cytogenetic Test in Cases without Ultrasound Abnormalities and Its Implementation in Clinical Practice. Issue 9 (6th June 2013) Authors: Srebniak, Malgorzata I.; Mout, Lisanne; Van Opstal, Diane; Galjaard, Robert‐Jan H. Journal: Human mutation Issue: Volume 34:Issue 9(2013:Sep.) Page Start: 1298 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Another Rare Prenatal Case of Post‐Zygotic Mosaic Trisomy 17. Issue 5 (20th March 2013) Authors: de Vries, Femke A.T.; Govaerts, Lutgarde C.P.; Knijnenburg, Jeroen; Knapen, Maarten F.C.M.; Oudesluijs, Grétel G.; Lont, Debora; Noomen, Petra; de Graaff, Katja; Srebniak, Malgorzata I.; Van Opstal, Diane Journal: American journal of medical genetics Issue: Volume 161:Issue 5(2013:May) Page Start: 1196 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Benefits and Burdens of Using a SNP Array in Pregnancies at Increased Risk for the Common Aneuploidies. Issue 3 (13th March 2015) Authors: Van Opstal, Diane; de Vries, Femke; Govaerts, Lutgarde; Boter, Marjan; Lont, Debora; van Veen, Stefanie; Joosten, Marieke; Diderich, Karin; Galjaard, Robert‐Jan; Srebniak, Malgorzata I. Journal: Human mutation Issue: Volume 36:Issue 3(2015:Mar.) Page Start: 319 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Benefits and Burdens of Using a SNP Array in Pregnancies at Increased Risk for the Common Aneuploidies. Issue 3 (March 2015) Authors: Van Opstal, Diane; de Vries, Femke; Govaerts, Lutgarde; Boter, Marjan; Lont, Debora; van Veen, Stefanie; Joosten, Marieke; Diderich, Karin; Galjaard, Robert‐Jan; Srebniak, Malgorzata I. Journal: Human mutation Issue: Volume 36:Issue 3(2015:Mar.) Page Start: 319 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Chromosomal mosaicism in human blastocysts: a cytogenetic comparison of trophectoderm and inner cell mass after next-generation sequencing. Issue 5 (November 2022) Authors: Chavli, Effrosyni; van den Born, Myrthe; Eleveld, Cindy; Boter, Marjan; van Marion, Ronald; Hoefsloot, Lies; Laven, Joop; Baart, Esther; Van Opstal, Diane Journal: Reproductive biomedicine online Issue: Volume 45:Issue 5(2022) Page Start: 867 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Clinical experience of unexpected findings in prenatal array testing. (August 2016) Authors: Joosten, Marieke; Diderich, Karin EM; Van Opstal, Diane; Govaerts, Lutgarde CP; Riedijk, Sam R; Prinsen, A Krista E; De Vries, Femke AT; Go, Attie TJI; Galjaard, Robert-Jan H; Srebniak, Malgorzata I Journal: Biomarkers in medicine Issue: Volume 10:Number 8(2016) Page Start: 831 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Cytogenetic confirmation of a positive NIPT result: evidence-based choice between chorionic villus sampling and amniocentesis depending on chromosome aberration. (3rd May 2016) Authors: Van Opstal, Diane; Srebniak, Malgorzata I Journal: Expert review of molecular diagnostics Issue: Volume 16:Number 5(2016) Page Start: 513 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Is carriership of a balanced translocation or inversion an indication for non-invasive prenatal testing?. (3rd June 2018) Authors: Srebniak, Malgorzata I.; Vogel, Ida; Van Opstal, Diane Journal: Expert review of molecular diagnostics Issue: Volume 18:Number 6(2018) Page Start: 477 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Is it feasible to select fetuses for prenatal WES based on the prenatal phenotype?. (10th September 2019) Authors: Diderich, Karin; Joosten, Marieke; Govaerts, Lutgarde; Van Opstal, Diane; Go, Attie; Knapen, Maarten; Galjaard, Robert‐Jan; Hoefsloot, Lies; Srebniak, Malgorzata Journal: Prenatal diagnosis Issue: Volume 39:Number 11(2019) Page Start: 1039 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Mosaic maternal 10qter deletions are associated with FRA10B expansions and may cause false-positive noninvasive prenatal screening results. (November 2018) Authors: Huijsdens–van Amsterdam, Karin; Straver, Roy; van Maarle, Merel; Knegt, Alida; Van Opstal, Diane; Sleutels, Frank; Smeets, Dominique; Sistermans, Erik Journal: Genetics in medicine Issue: Volume 20:Number 11(2018) Page Start: 1472 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗