A Qualitative Study of Healthcare Providers’ Perspectives on the Implications of Genome-Wide Testing in Pediatric Clinical Practice
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Link
http://link.springer.com/content/pdf/10.1007/s10897-013-9653-8
Reference54 articles.
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2. Ali-Khan, S. E., Daar, A. S., Shuman, C., Ray, P. N., & Scherer, S. W. (2009). Whole genome scanning: Resolving clinical diagnosis and management amidst complex data. Pediatric Research, 66(4), 357–363.
3. Aronson, S. J., Clark, E. H., Varugheese, M., Baxter, S., Babb, L. J., & Rehm, H. L. (2012). Communicating new knowledge on previously reported genetic variants. Genetics in Medicine, 14(8), 713–719.
4. Bazeley, P. (2007). Qualitative analysis with Nvivo. Thousand Oaks: Sage Publications Ltd.
5. Beaudet, A. L., & Belmont, J. W. (2008). Array-based DNA diagnostics: Let the revolution begin. Annu. Rev. Med., 59, 113–129.
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