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May 15, 2009 (Vol. 29, No. 10)

CGH Sheds Its Light on Disease Etiology

Diseases that Have Defied Description Can Now Be Described and Explained

  • Array comparative genomic hybridization (CGH) is illuminating DNA copy number variations (CNV) throughout the genome to diagnose disease etiology and to help tailor treatment regimens for patients to improve health outcomes. In January 2007, the College of American Pathologists and American Society of Clinical Oncology (CAP/ASCO) published guideline ...

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