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Whole-exome sequencing for finding de novo mutations in sporadic mental retardation

Genome Biology (2010) 11(12)
DOI: 10.1186/gb-2010-11-12-144
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Abstract

Recent work has used a family-based approach and whole-exome sequencing to identify de novo mutations in sporadic cases of mental retardation © 2010 BioMed Central Ltd.

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Robinson, P. N. (2010). Whole-exome sequencing for finding de novo mutations in sporadic mental retardation. Genome Biology, 11(12). https://doi.org/10.1186/gb-2010-11-12-144

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