1. All‐in‐one whole exome sequencing strategy with simultaneous copy number variant, single nucleotide variant and absence‐of‐heterozygosity analysis in fetuses with structural ultrasound anomalies: A 1‐year experience. (5th February 2023) Authors: Faas, Brigitte H. W.; Westra, Dineke; de Munnik, Sonja A.; van Rij, Maartje; Marcelis, Carlo; Joosten, Sara; Krapels, Ingrid; Vernimmen, Vivian; Heijligers, Malou; Willemsen, Marjolein H.; de Leeuw, Nicole; Rinne, Tuula; Pfundt, Rolph; Smeekens, Sanne P.; Stegmann, Sander P. A.; Macville, Merryn;... Journal: Prenatal diagnosis Issue: Volume 43:Number 4(2023) Page Start: 527 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Benefits and limitations of whole genome versus targeted approaches for noninvasive prenatal testing for fetal aneuploidies. (17th May 2013) Authors: Boon, Elles M. J.; Faas, Brigitte H. W.; Chitty, Lyn S.; Bianchi, Diana W. Journal: Prenatal diagnosis Issue: Volume 33:Number 6(2013:Jun.) Page Start: 563 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Comment on 'Confined placental mosaicism: implications for fetal chromosomal analysis using microarray comparative genomic hybridization'. (August 2014) Authors: Kooper, Angelique J. A.; Faas, Brigitte H. W. Journal: Prenatal diagnosis Issue: Volume 34:Number 8(2014:Aug.) Page Start: 815 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Current controversies in prenatal diagnosis 1: NIPT for chromosome abnormalities should be offered to women with low a priori risk1. (January 2015) Authors: Van Lith, Jan M. M.; Faas, Brigitte H. W.; Bianchi, Diana W. Journal: Prenatal diagnosis Issue: Volume 35:Number 1(2015:Jan.) Page Start: 8 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Detecting fetal subchromosomal aberrations by MPS: an unexpected discrepancy between amniocyte DNA and ccffDNA. (6th February 2014) Authors: Buysse, Karen; de, Joep; Janssen, Irene M.; van, Bregje W. M.; Gomes, Ingrid; Hehir‐Kwa, Jayne; Eggink, Alex J.; van, John M. G.; Vissers, Lisenka E. L. M.; Geurts van Kessel, Ad; Faas, Brigitte H. W. Journal: Prenatal diagnosis Issue: Volume 34:Number 4(2014:Apr.) Page Start: 402 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. In case you missed it: the Prenatal Diagnosis section editors bring you the most significant advances of 2013. (January 2014) Authors: Bianchi, Diana W.; Van Mieghem, Tim; Shaffer, Lisa G.; Faas, Brigitte H. W.; Chitty, Lyn S.; Ghidini, Alessandro; Deprest, Jan Journal: Prenatal diagnosis Issue: Volume 34:Number 1(2014:Jan.) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Summary of the ISPD Preconference Day, June 3, 2012, Miami Beach1. (7th November 2012) Authors: Faas, Brigitte H. W.; Odibo, Anthony O.; Cirigliano, V.; Schielen, P.; Pergament, D.; Devers, P.; Oepkes, D.; Benn, P. Journal: Prenatal diagnosis Issue: Volume 33:Number 1(2013:Jan.) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. The 2013 Malcolm Ferguson‐Smith Young Investigator Award. (August 2014) Authors: Bianchi, Diana W.; Chitty, Lyn S.; Deprest, Jan; Faas, Brigitte H. W.; Ghidini, Alessandro; Cousens, Rupert K. J. Journal: Prenatal diagnosis Issue: Volume 34:Number 8(2014:Aug.) Page Start: 717 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. The 2014 Malcolm Ferguson‐Smith Young Investigator Award. (June 2015) Authors: Bianchi, Diana W.; Chitty, Lyn S.; Deprest, Jan; Faas, Brigitte H. W.; Ghidini, Alessandro; Cousens, Rupert K. J. Journal: Prenatal diagnosis Issue: Volume 35:Number 6(2015:Jun.) Page Start: 515 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Validation of two‐channel sequencing‐by‐synthesis for noninvasive prenatal testing of fetal whole and partial chromosome aberrations. (15th February 2016) Authors: Neveling, Kornelia; Tjwan Thung, Djie; Beulen, Lean; van Rens‐Buijsman, Wendy; Gomes, Ingrid; van den Heuvel, Simone; Mieloo, Hanneke; Derks‐Prinsen, Irma; Kater‐Baats, Ellen; Faas, Brigitte H. W. Journal: Prenatal diagnosis Issue: Volume 36:Number 3(2016) Page Start: 216 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗