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  Vol. 299 No. 11, March 19, 2008 TABLE OF CONTENTS
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Genetics and Genomics for Clinicians

Phil B. Fontanarosa, MD, MBA; Boris Pasche, MD, PhD; Catherine D. DeAngelis, MD, MPH

JAMA. 2008;299(11):1364-1365.

Since this article does not have an abstract, we have provided the first 150 words of the full text and any section headings.

Advances in genetics and genomics are revolutionizing biomedical science and providing great promise for the future of clinical practice. The magnitude, scope, and pace of discovery in genetics and genomics research are at unprecedented levels and continue to increase exponentially. Progress in basic science resulting from the sequencing of the human genome1 and new approaches for genomics analyses have accelerated and continue to expand, resulting in new knowledge, mechanisms, and techniques for examining the genetic basis of disease. These discoveries have important implications for understanding disease processes and pathophysiology, for predicting disease susceptibility and progression, and for refining and individualizing treatments—all of which ultimately have the potential to improve health and to increase both quality of life and longevity.

Given the pace of discovery and the promise in translating these scientific discoveries to clinical application, physicians . . . [Full Text of this Article]

Author Affiliations: Dr Fontanarosa (phil.fontanarosa@jama-archives.org) is Executive Deputy Editor, Dr Pasche is Contributing Editor, and Dr DeAngelis is Editor in Chief, JAMA.







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