1. Mild β+-Thalassemia Associated With Two Linked Sequence Variants: IVS-II-839 (T>C) and IVS-II-844 (C>A). (August 2013) Authors: Waye, John S.; Eng, Barry; Hellens, Laurie; Hohenadel, Betty-Ann; Nakamura, Lisa M.; Walker, Lynda Journal: Hemoglobin Issue: Volume 37:Number 4(2013) Page Start: 378 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Normal Hb A2 β-Thalassemia Trait: Frameshift Mutation (HBB: c.187_251dup) in Cis with the Hb A2' δ-Globin Gene Missense Mutation (HBD: c.49G>C). (April 2013) Authors: Waye, John S.; Eng, Barry; Hellens, Laurie; Hohenadel, Betty-Ann; Nakamura, Lisa M.; Walker, Lynda Journal: Hemoglobin Issue: Volume 37:Number 2(2013) Page Start: 201 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Sudanese (δβ)0-Thalassemia: Identification and Characterization of a Novel 9.6 kb Deletion. (3rd September 2015) Authors: Waye, John S.; Eng, Barry; Got, Tiffany; Hanna, Meredith; Hohenadel, Betty-Ann; Nakamura, Lisa M.; Walker, Lynda Journal: Hemoglobin Issue: Volume 39:Number 5(2015) Page Start: 368 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Α+-Thalassemia Due to a Frameshift Mutation of the α2-Globin Gene [codons 55/56 (+T) or HBA2: c.168dup]. (June 2015) Authors: Waye, John S.; Eng, Barry; Hanna, Meredith; Hohenadel, Betty-Ann; Nakamura, Lisa M.; Walker, Lynda Journal: Hemoglobin Issue: Volume 39:Number 3(2015) Page Start: 209 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗