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Related terms include personalized medicine, precision medicine, companion diagnostics, molecular diagnostics.
To assist in the identification of genetic mutations in humans with implications regarding health and treatment decisions; to assist in the identification of pathogenic organisms.
There are no food, fluid, activity, or medication restrictions unless by medical direction.
Method: Methods are specific to the study of interest and preferred specimen type. Methods include polymerase chain reaction (PCR), immunohistochemical assay, DNA probe using fluorescence in situ hybridization (FISH), gene amplification using chromogenic in situ hybridization (CISH), and cell culture with karyotyping. Absence of findings consistent with genetic abnormalities related to disease or the ability to metabolize medications normally.
Critical Findings and Potential Interventions
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Bladh, Mickey Lynn., and Anne M. Van Leeuwen. "Genetic Testing." Davis's Lab & Diagnostic Tests, 7th ed., F.A. Davis Company, 2017. Nursing Central, nursing.unboundmedicine.com/nursingcentral/view/Davis-Lab-and-Diagnostic-Tests/425432/all/Genetic_Testing.
Bladh ML, Van Leeuwen AM. Genetic Testing. Davis's Lab & Diagnostic Tests. 7th ed. F.A. Davis Company; 2017. https://nursing.unboundmedicine.com/nursingcentral/view/Davis-Lab-and-Diagnostic-Tests/425432/all/Genetic_Testing. Accessed November 21, 2019.
Bladh, M. L., & Van Leeuwen, A. M. (2017). Genetic Testing. In Davis's Lab & Diagnostic Tests. Available from https://nursing.unboundmedicine.com/nursingcentral/view/Davis-Lab-and-Diagnostic-Tests/425432/all/Genetic_Testing
Bladh ML, Van Leeuwen AM. Genetic Testing [Internet]. In: Davis's Lab & Diagnostic Tests. F.A. Davis Company; 2017. [cited 2019 November 21]. Available from: https://nursing.unboundmedicine.com/nursingcentral/view/Davis-Lab-and-Diagnostic-Tests/425432/all/Genetic_Testing.
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