1. A Novel Deletion in SMPX Causes a Rare form of X‐Linked Progressive Hearing Loss in Two Families Due to a Founder Effect. Issue 1 (11th October 2012) Authors: Abdelfatah, Nelly; Merner, Nancy; Houston, Jim; Benteau, Tammy; Griffin, Anne; Doucette, Lance; Stockley, Tracy; Lauzon, Julie L.; Young, Terry‐Lynn Journal: Human mutation Issue: Volume 34:Issue 1(2013:Jan.) Page Start: 66 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Molecular Genetics of Achromatopsia in Newfoundland Reveal Genetic Heterogeneity, Founder Effects and the First Cases of Jalili Syndrome in North America. (September 2013) Authors: Doucette, Lance; Green, Jane; Black, Coleman; Schwartzentruber, Jeremy; Johnson, Gordon J.; Galutira, Dante; Young, Terry-Lynn Journal: Ophthalmic genetics Issue: Volume 34:Number 3(2013:Sep.) Page Start: 119 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗