Genetic Counselors’ Views and Experiences with the Clinical Integration of Genome Sequencing
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Link
http://link.springer.com/content/pdf/10.1007/s10897-014-9709-4
Reference31 articles.
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3. Bras, J., Guerreiro, R., & Hardy, J. (2012). Use of next-generation sequencing and other whole-genome strategies to dissect neurological disease. Nature Reviews Neuroscience, 13(7), 453–464.
4. Brunham, L. R., & Hayden, M. R. (2012). Medicine. Whole-genome sequencing: the new standard of care? Science, 336(6085), 1112–1113.
5. Burniat, A., Pirson, I., Vilain, C., Kulik, W., Afink, G., Moreno-Reyes, R., et al. (2012). Iodotyrosine deiodinase defect identified via genome-wide approach. The Journal of Clinical Endocrinology and Metabolism, 97(7), 1276–1283.
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