1. A study of elective genome sequencing and pharmacogenetic testing in an unselected population. Issue 9 (27th July 2021) Authors: Cochran, Meagan; East, Kelly; Greve, Veronica; Kelly, Melissa; Kelley, Whitley; Moore, Troy; Myers, Richard M.; Odom, Katherine; Schroeder, Molly C.; Bick, David Journal: Molecular genetics & genomic medicine Issue: Volume 9:Issue 9(2021) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. High Incidence of Noonan Syndrome Features Including Short Stature and Pulmonic Stenosis in Patients carrying NF1 Missense Mutations Affecting p.Arg1809: Genotype–Phenotype Correlation. Issue 11 (21st August 2015) Authors: Rojnueangnit, Kitiwan; Xie, Jing; Gomes, Alicia; Sharp, Angela; Callens, Tom; Chen, Yunjia; Liu, Ying; Cochran, Meagan; Abbott, Mary‐Alice; Atkin, Joan; Babovic‐Vuksanovic, Dusica; Barnett, Christopher P.; Crenshaw, Melissa; Bartholomew, Dennis W.; Basel, Lina; Bellus, Gary; Ben‐Shachar, Shay; Bi... Journal: Human mutation Issue: Volume 36:Issue 11(2015:Nov.) Page Start: 1052 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Understanding the present and preparing for the future: Exploring the needs of diagnostic and elective genomic medicine patients. Issue 2 (9th April 2019) Authors: East, Kelly M.; Cochran, Meagan; Kelley, Whitley V.; Greve, Veronica; Emmerson, Kristina; Raines, Grace; Cochran, Jesse Nicholas; Hott, Adam M.; Bick, David Journal: Journal of genetic counseling Issue: Volume 28:Issue 2(2019) Page Start: 438 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗