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Author/Creator Cochran, Meagan

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
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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
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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
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Available online (eLD content is only available in our Reading Rooms) ↗