Understanding genetic testing in primary care

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Authors
Seiler, Brittany
Advisors
Brown, Gina
Issue Date
2016-04-29
Type
Abstract
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Research Projects
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Citation
Seiler, Brittany. 2016. Understanding genetic testing in primary care. --In Proceedings: 12th Annual Symposium on Graduate Research and Scholarly Projects. Wichita, KS: Wichita State University, p. 98
Abstract

As genetic tests are expanding, primary care providers have an increasing need to integrate tests into their practice. The purpose of this project is to offer an evidence-based clinical review, regarding types of genetic tests and their application in primary care. Practical information on the utilization of karyotype, microarray, polymerase chain reaction, fluorescence in situ hybridization, and whole exome sequencing were searched. Karyotype and microarray can be used when considering pediatric disorders. PCR is most useful for infectious processes, while FISH has a niche with malignancies. Finally, WES is best used when other diagnostic avenues have been inconclusive or unrevealed disorders. The article was submitted for publication at JAAPA to provide a needed resource in appropriately utilizing genetic testing in primary care.

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Description
Presented to the 12th Annual Symposium on Graduate Research and Scholarly Projects (GRASP) held at the Heskett Center, Wichita State University, April 29, 2016.
Research completed at Department of Physician Assistant, College of Health Professions
Publisher
Wichita State University
Journal
Book Title
Series
GRASP
v. 12
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