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March 16, 2012Journal of Molecular DiagnosticsOpen Access

Assessment of Target Enrichment Platforms Using Massively Parallel Sequencing for the Mutation Detection for Congenital Muscular Dystrophy

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Authors

CVC. Alexander ValenciaDRDevin RhodenizerSBShruti Bhide

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Valencia et al. (2012) studied this question.

synapsesocial.com/papers/6a7863764fe2e6ffd8ed6599https://doi.org/10.1016/j.jmoldx.2012.01.009
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Also Consider

Synapse has enriched 3 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Massively parallel sequencing of ataxia genes after array-based enrichment2010 · 105 citations
  2. 2Next-generation sequencing: applications beyond genomes2008 · 129 citations
  3. 3Consensus Statement on Standard of Care for Congenital Muscular Dystrophies2010 · 218 citations