1. Identification of clinically significant, submicroscopic chromosome alterations and UPD in fetuses with ultrasound anomalies using genome-wide 250k SNP array analysis. Issue 9 (24th June 2010) Authors: Faas, B H W; van der Burgt, I; Kooper, A J A; Pfundt, R; Hehir-Kwa, J Y; Smits, A P T; de Leeuw, N Journal: Journal of medical genetics Issue: Volume 47:Issue 9(2010) Page Start: 586 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗