Array-based FMR1 sequencing and deletion analysis in patients with a fragile X syndrome-like phenotype.

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Published in PLoS One on March 05, 2010

Authors

Stephen C Collins1, Brad Coffee, Paul J Benke, Elizabeth Berry-Kravis, Fred Gilbert, Ben Oostra, Dicky Halley, Michael E Zwick, David J Cutler, Stephen T Warren

Author Affiliations

1: Department of Human Genetics, Emory University School of Medicine, Atlanta, Georgia, United States of America.

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