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MLGA: a cost-effective approach to the diagnosis of gene deletions in eye development anomalies
Molecular Vision, 07/29/09
Wyatt AW et al. – The authors used the new selector technique, MLGA, to confirm deletions in two genes, SOX2 and OTX2, in individuals with developmental eye disease. The authors conclude that MLGA has the potential to be a useful technique in diagnostic research for the identification of deletions or duplications of known genes due to its speed and relatively low cost.
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