Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
4095401 | Spine Deformity | 2014 | 9 Pages |
Abstract
These data underscore the usefulness of updated genetic evaluations including high-density microarray-based genotyping and other next-generation methods in patients with unexplained EOS, even when prior genetic studies were negative. These data also suggest the intriguing possibility that other mutations detectable by whole genome sequencing, as well as epigenetic effects, await discovery in the EOS population.
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Authors
Xiaochong MS, MD, Garrett MD, Karl MD, Charles MD, Steven MD, Carol A. PhD,