1. Array CGH as a first-tier test for neonates with congenital heart disease. (6th November 2013) Authors: Bachman, Kristine K.; DeWard, Stephanie J.; Chrysostomou, Constantinos; Munoz, Ricardo; Madan-Khetarpal, Suneeta Journal: Cardiology in the young Issue: Volume 25:Number 1(2015) Page Start: 115 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Practical Aspects of Recruitment and Retention in Clinical Trials of Rare Genetic Diseases: The Phenylketonuria (PKU) Experience. Issue 1 (8th September 2013) Authors: DeWard, Stephanie J.; Wilson, Ashley; Bausell, Heather; Volz, Ashley S.; Mooney, Kimberly Journal: Journal of genetic counseling Issue: Volume 23:Issue 1(2014) Page Start: 20 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Three Supernumerary Marker Chromosomes in a Patient with Developmental Delay, Mental Retardation, and Dysmorphic Features. (15th June 2011) Authors: Hu, Jie; Madan-Khetarpal, Suneeta; Serrano Russi, Alvaro H.; Kochmar, Sally; DeWard, Stephanie J.; Sathanoori, Malini; Surti, Urvashi Other Names: Toydemir Reha Academic Editor. Journal: Genetics research international Issue: Volume 2011(2011) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗